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D029424: Pulmonary Disease, Chronic Obstructive

Developed by Shray Alag, The Harker School
Sections: Correlations, Clinical Trials, and HPO

Correlations computed by analyzing all clinical trials.

Navigate: Clinical Trials and HPO


Correlated Drug Terms (18)


Name (Synonyms) Correlation
drug3801 control group Wiki 0.38
drug1410 HCFWO Wiki 0.38
drug3169 Standard Care Plus Monitoring Wiki 0.38
Name (Synonyms) Correlation
drug3835 exercise group Wiki 0.38
drug3001 Saliva specimen Wiki 0.38
drug1313 Fingerstick Wiki 0.38
drug3171 Standard Donor Plasma Wiki 0.38
drug1250 Exposure to telemedicine, after the onset of the pandemic Wiki 0.38
drug2145 Nasal Swab Wiki 0.38
drug1304 Fenofibrate Wiki 0.38
drug3412 Throat swab Wiki 0.27
drug3560 Usual care Wiki 0.22
drug367 BCG vaccine Wiki 0.19
drug425 Best Practice Wiki 0.17
drug2152 Nasopharyngeal swab Wiki 0.14
drug884 Convalescent Plasma Wiki 0.07
drug3430 Tocilizumab Wiki 0.06
drug2490 Placebo Wiki 0.03

Correlated MeSH Terms (16)


Name (Synonyms) Correlation
D008173 Lung Diseases, Obstructive NIH 0.80
D003139 Common Cold NIH 0.27
D003327 Coronary Disease NIH 0.19
Name (Synonyms) Correlation
D003324 Coronary Artery Disease NIH 0.19
D007676 Kidney Failure, Chronic NIH 0.17
D006331 Heart Diseases NIH 0.14
D006333 Heart Failure NIH 0.13
D020521 Stroke NIH 0.10
D008171 Lung Diseases, NIH 0.08
D009369 Neoplasms, NIH 0.07
D012141 Respiratory Tract Infections NIH 0.06
D007239 Infection NIH 0.05
D014777 Virus Diseases NIH 0.04
D045169 Severe Acute Respiratory Syndrome NIH 0.03
D003141 Communicable Diseases NIH 0.03
D018352 Coronavirus Infections NIH 0.03

Correlated HPO Terms (7)


Name (Synonyms) Correlation
HP:0006510 Chronic pulmonary obstruction HPO 0.93
HP:0006536 Pulmonary obstruction HPO 0.71
HP:0001677 Coronary artery atherosclerosis HPO 0.19
Name (Synonyms) Correlation
HP:0001297 Stroke HPO 0.10
HP:0002088 Abnormal lung morphology HPO 0.08
HP:0002664 Neoplasm HPO 0.07
HP:0011947 Respiratory tract infection HPO 0.06

Clinical Trials

Navigate: Correlations   HPO

There are 7 clinical trials


1 Audio Data Collection for Identification and Classification of Coughing

An open access study that will define and collect digital measures of coughing in multiple populations and public spaces using various means of audio data collection.

NCT04326309
Conditions
  1. COVID-19
  2. Coronavirus Infections
  3. Hay Fever
  4. Asthma
  5. Chronic Obstructive Pulmonary Disease
  6. Influenza
  7. Common Cold
  8. Respiratory Tract Infections
  9. Healthy
MeSH:Infection Communicable Diseases Respiratory Tract Infections Coronavirus Infections Severe Acute Respiratory Syndrome Common Cold Lung Diseases, Obstructive Pulmonary Disease, Chronic Obstructive
HPO:Chronic pulmonary obstruction Pulmonary obstruction Respiratory tract infection

Primary Outcomes

Description: Size of collected audio dataset measured as number of collected cough sounds, targeting ≥10,000 identified coughs.

Measure: Dataset size

Time: 14 days

Secondary Outcomes

Description: Identification of cough sounds by the existing mathematical model with ≥ 99% specificity and ≥ 60% sensitivity

Measure: Cough sound identification

Time: 14 days

Description: Increase in the sensitivity of the mathematical model to cough sounds to ≥ 70% while retaining the specificity of ≥ 99%

Measure: Improvement of the existing model

Time: 14 days

Description: Determination of the level of acceptance and satisfaction of the solution by patients by means of a Standard Usability Questionnaire to provide feedback. The score ranges from 10 to 50, higher score indicating a better usability.

Measure: Evaluate the usability of the application

Time: 14 days
2 Tociluzumab for Cytokine Release Syndrome With SARS-CoV-2: An Open-Labeled, Randomized Phase 3 Trial

This phase III trial compares the effect of adding tocilizumab to standard of care versus standard of care alone in treating cytokine release syndrome (CRS) in patients with SARS-CoV-2 infection. CRS is a potentially serious disorder caused by the release of an excessive amount of substance that is made by cells of the immune system (cytokines) as a response to viral infection. Tocilizumab is used to decrease the body's immune response. Adding tocilizumab to standard of care may work better in treating CRS in patients with SARS-CoV-2 infection compared to standard of care alone.

NCT04361552
Conditions
  1. Cerebrovascular Accident
  2. Chronic Obstructive Pulmonary Disease
  3. Chronic Renal Failure
  4. Coronary Artery Disease
  5. Diabetes Mellitus
  6. Malignant Neoplasm
  7. SARS Coronavirus 2 Infection
Interventions
  1. Other: Best Practice
  2. Biological: Tocilizumab
MeSH:Infection Neoplasms Lung Diseases, Obstructive Pulmonary Disease, Chronic Obstructive Stroke Kidney Failure, Chronic Coronary Artery Disease
HPO:Chronic pulmonary obstruction Coronary artery atherosclerosis Neoplasm Pulmonary obstruction Stroke

Primary Outcomes

Description: The 7-day length of invasive MV for each arm will be estimated with 95% confidence intervals (CIs) using the exact binomial distribution. Their difference by the arms will be tested by Cochran-Mantel-Haenszel (CMH) test stratified by the age group and Sequential Organ Failure Assessment (SOFA) score at significance level of 0.05.

Measure: 7-day length of invasive mechanical ventilation (MV)

Time: Up to 7 days

Description: Defined as death within 30-day after randomization. The 30-day mortality rate for each arm will be estimated with 95% CIs using the exact binomial distribution. Their difference by the arms will be tested CMH test stratified by the age group and SOFA score at significance level of 0.05.

Measure: 30-day mortality rate

Time: Up to 30-day after randomization

Secondary Outcomes

Description: The rate of ICU transfer for each arm will be estimated with 95% CIs using the exact binomial distribution. Their difference by the arms will be tested CMH test stratified by the age group and SOFA score at significance level of 0.05.

Measure: Rate of intensive care (ICU) transfer

Time: Up to 2 years

Description: The rate of invasive mechanical ventilation for each arm will be estimated with 95% CIs using the exact binomial distribution. Their difference by the arms will be tested CMH test stratified by the age group and SOFA score at significance level of 0.05.

Measure: Rate of invasive mechanical ventilation

Time: Up to 2 years

Description: The rate of tracheostomy for each arm will be estimated with 95% CIs using the exact binomial distribution. Their difference by the arms will be tested CMH test stratified by the age group and SOFA score at significance level of 0.05.

Measure: Rate of tracheostomy

Time: Up to 2 years

Description: Will first be described by median and inter-quartile, and then compared between two arms by Wilcoxon Sum-Rank test

Measure: Length of ICU stay

Time: Up to 2 years

Measure: Length of hospital stay

Time: Up 2 years
3 Cross-Sectional Observation Telephone Survey Study to Understand the Changes in COPD Exacerbation Patterns and Potential Causes of These During the COVID-19 Pandemic

This cross-sectional observational study will collect information about changes in exacerbation frequency and behaviour amongst a clinical cohort of severe or complex COPD clinic patients. This will be done through a combination of telephone survey and access to electronic heath records.

NCT04407598
Conditions
  1. COPD Exacerbation
  2. COPD
MeSH:Pulmonary Disease, Chronic Obstructive
HPO:Chronic pulmonary obstruction

Primary Outcomes

Description: The primary outcome will be the change in number of moderate or severe AECOPD events over the 46 days from the 15th March, 2020 to 30th April, 2020 compared to the same 46 day period in 2019.

Measure: Change in COPD Exacerbation Rate

Time: 46 days

Secondary Outcomes

Measure: Change in number of Severe AECOPD events during period of interest in 2020 from same period in 2019.

Time: 46 days

Measure: Change in Moderate AECOPD events during period of interest in 2020 from same period in 2019.

Time: 46 days

Measure: Social contact changes during i) pre-lockdown and ii) lockdown period

Time: 46 days

Measure: Household contacts during i) pre-lockdown and ii) lockdown period

Time: 46 days

Measure: Household visitors during i) pre-lockdown and ii) lockdown period

Time: 46 days

Measure: Regular shopping behaviour during i) pre-lockdown and ii) lockdown period

Time: 46 days

Measure: Medication changes during i) pre-lockdown and ii) lockdown period

Time: 46 days

Measure: Reported change in regular medication usage during i) pre-lockdown and ii) lockdown period

Time: 46 days

Measure: Change in physical activity levels during i) pre-lockdown and ii) lockdown period

Time: 46 days

Measure: Change in anxiety levels during i) pre-lockdown and ii) lockdown period

Time: 46 days

Measure: Perceived fear of hospitalisation during COVID-19 period

Time: 46 days

Measure: Patient reported changes in perception of symptoms, need for hospitalisation and availability and safety of healthcare resources thought semi-structured interviews in 20 patients (nested qualitative study)

Time: 46 days

Measure: Association between changes in AECOPD event rate and changes in local air pollution during the COVID-19 lockdown

Time: 46 days
4 A Randomized Clinical Trial for Enhanced Trained Immune Responses Through Bacillus Calmette-Guérin Vaccination to Prevent Infections by COVID-19: The ACTIVATE II Trial

Based on findings of the interim analysis of the ACTIVATE study showing 53% decrease of the incidence of all new infections with BCG vaccination, a new trial is designed aiming to validate if BCG can protect against COVID-19 (Corona Virus Disease-19).The aim of the study is to demonstrate in a double-blind, placebo-controlled approach if vaccination of participants susceptible to COVID-19 with BCG vaccine may modulate their disease susceptibility for COVID-19. This will be validated using both clinical and immunological criteria. At the same time, a sub-study will be conducted and the mechanism of benefit from BCG vaccination by assessing its effect on vascular endothelial function and mononuclear blood cells will be studied

NCT04414267
Conditions
  1. COVID-19
  2. Virus Diseases
  3. Corona Virus Infection
  4. Coronary Heart Disease
  5. Chronic Obstructive Pulmonary Disease
Interventions
  1. Biological: BCG vaccine
  2. Biological: Placebo
MeSH:Infection Virus Diseases Coronavirus Infections Severe Acute Respiratory Syndrome Lung Diseases, Obstructive Pulmonary Disease, Chronic Obstructive Heart Diseases Coronary Disease
HPO:Chronic pulmonary obstruction Pulmonary obstruction

Primary Outcomes

Description: This is set on visit 3 (90 ± 5 days from the date of visit 1). The two groups of vaccination are compared for the primary endpoints which is composite. Patients who meet any of the following will be considered to meet the primary endpoint: Positive for the respiratory questionnaire endpoint when at least one of the following combination is met either at visit 2 and/or at visit 3: One situation definitively related to COVID-19 All four questions of symptoms possibly related to COVID-19 At least two questions of symptoms possibly related to COVID-19 as well as need for admission at the emergency department of any hospital and/or need for intake of antibiotics At least four questions of symptoms probably related to COVID-19 one of which is "need for admission at the emergency department of any hospital and/or need for intake of antibiotics" Positive IgG or IgM antibodies against SARS-CoV-2

Measure: Positive for the respiratory questionnaire consisted of questions concerning the appearance of symptoms possibly, probably and/or definitively related to COVID-19 on visit 3.

Time: Visit 3 (90 +/- 5 days)

Secondary Outcomes

Description: The two groups of vaccination are compared for the primary endpoints which is composite (as defined at primary study endpoint) and meet a positive respiratory questionnaire endpoint on visit 4

Measure: Positive respiratory questionnaire endpoint consisted of questions concerning the appearance of symptoms possibly, probably and/or definitively related to COVID-19 on visit 4

Time: Visit 4 (135 +/- 5 days)

Description: The two groups of vaccination are compared for the primary endpoints which is composite (as defined at primary study endpoint) and meet a positive respiratory questionnaire endpoint (as defined at primary study endpoint) on visit 5

Measure: Positive respiratory questionnaire endpoint consisted of questions concerning the appearance of symptoms possibly, probably and/or definitively related to COVID-19 on visit 5

Time: Visit 5 (180 +/- 5 days)

Description: Prevalence of IgG/IgM against SARS-CoV-2 will be measured among the patients who failed the eligibility procedure and the patients that were eligible and were enrolled

Measure: Prevalence of IgG/IgM against SARS-CoV-2

Time: Screening Visit and Visit 3 (90 +/- 5 days)

Description: Itemized analysis of each of the components of the respiratory questionnaire on each study visit

Measure: Analysis of each of the components of the respiratory questionnaire consisted of questions concerning the appearance of symptoms possibly, probably and/or definitively related to COVID-19.

Time: Visit 2 (45 +/- 5 days), Visit 3 (90 +/- 5 days), Visit 4 (135 +/- 5 days), Visit 5 (180 +/- 5 days)

Description: The impact of new cardiovascular events between the two study groups (placebo and BCG) will be analyzed, though the collection of any cardiovascular events occured to the enrolled patients.

Measure: The impact of new cardiovascular events between the two study groups

Time: Visit 2 (45 +/- 5 days), Visit 3 (90 +/- 5 days), Visit 4 (135 +/- 5 days), Visit 5 (180 +/- 5 days)

Description: Differences in repeated measurements of arterial stiffness in visit 3 between the two sub-study groups (placebo or BCG) will be analyzed through the speed of the pulse wave velocity. Pulse wave velocity is measured in m/sec.

Measure: Differences in repeated measurements of angiometric parameters (arterial hardness) between the two sub-study groups in Visit 3

Time: Visit 1 (Day 0), Visit 3 (90 +/- 5 days)

Description: Differences in repeated measurements of central arterial pressures and reflected waves in visit 3 between the two sub-study groups (placebo or BCG) will be measured non-invasively by pulse wave analysis. Central arterial pressure is measured in mmHg.

Measure: Differences in repeated measurements of angiometric parameters (central arterial pressures and reflected waves) between the two sub-study groups in Visit 3

Time: Visit 1 (Day 0), Visit 3 (90 +/- 5 days)

Description: Differences in repeated measurements of endothelial function in visit 3 between the two sub-study groups (placebo or BCG) will be measured by ultrasound measurement of endothelium-dependent flow-mediated dilatation and by nitrate-mediated dialatation. Endothelial function will be assessed by Flow Mediated Dilatation (FMD). Endothelium-dependent: diameter of the artery prior and after temporary ischemia in is measured in mm, nitrate-mediated: diameter of the artery prior and after nitrate administration is measured in mm

Measure: Differences in repeated measurements of angiometric parameters (endothelial function) between the two sub-study groups in Visit 3

Time: Visit 1 (Day 0), Visit 3 (90 +/- 5 days)

Description: Differences in repeated measurements of thickness of the medial carotid sheath in visit 3 between the two sub-study groups (placebo or BCG) will be measured by B-mode ultrasound examination. Intima-Media Thickness is measured in mm

Measure: Differences in repeated measurements of angiometric parameters (thickness of the medial carotid sheath) between the two sub-study groups in Visit 3

Time: Visit 1 (Day 0), Visit 3 (90 +/- 5 days)

Description: Differences in repeated measurements of arterial stiffness in visit 5 between the two sub-study groups (placebo or BCG) will be analyzed through the speed of the pulse wave velocity. Pulse wave velocity is measured in m/sec.

Measure: Differences in repeated measurements of angiometric parameters (arterial hardness) between the two sub-study groups in Visit 5

Time: Visit 1 (Day 0), Visit 3 (90 +/- 5 days), Visit 5 (180 +/- 5 days)

Description: Differences in repeated measurements of central arterial pressures and reflected waves in visit 5 between the two sub-study groups (placebo or BCG) will be measured non-invasively by pulse wave analysis. Central arterial pressure is measured in mmHg.

Measure: Differences in repeated measurements of angiometric parameters (central arterial pressures and reflected waves) between the two sub-study groups in Visit 5

Time: Visit 1 (Day 0), Visit 3 (90 +/- 5 days), Visit 5 (180 +/- 5 days)

Description: Differences in repeated measurements of thickness of the medial carotid sheath in visit 5 between the two sub-study groups (placebo or BCG) will be measured by B-mode ultrasound examination. Intima-Media Thickness is measured in mm

Measure: Differences in repeated measurements of angiometric parameters (thickness of the medial carotid sheath) between the two sub-study groups in Visit 5

Time: Visit 1 (Day 0), Visit 3 (90 +/- 5 days), Visit 5 (180 +/- 5 days)

Description: Differences in repeated measurements of endothelial function in visit 5 between the two sub-study groups (placebo or BCG) will be measured by ultrasound measurement of endothelium-dependent flow-mediated dilatation and by nitrate-mediated dialatation. Endothelial function will be assessed by Flow Mediated Dilatation (FMD). Endothelium-dependent: diameter of the artery prior and after temporary ischemia in is measured in mm, nitrate-mediated: diameter of the artery prior and after nitrate administration is measured in mm

Measure: Differences in repeated measurements of angiometric parameters (endothelial function) between the two sub-study groups in Visit 5

Time: Visit 1 (Day 0), Visit 3 (90 +/- 5 days), Visit 5 (180 +/- 5 days)

Description: Differences in cardiac ultrasound at visit 5 between the two sub-study groups (placebo or BCG) will be assessed using standard measurements from 2-D and Doppler echocardiography.

Measure: Differences in cardiac ultrasound at visit 5 between the two sub-study groups

Time: Visit 1 (Day 0), Visit 3 (90 +/- 5 days), Visit 5 (180 +/- 5 days)

Description: Changes in the release of cytokines from blood mononuclear cells at visit 3 between the two sub-study groups (placebo or BCG) will be analyzed

Measure: Changes in the release of cytokines from blood mononuclear cells at visit 3 between the two sub-study groups

Time: Visit 1 (Day 0), Visit 3 (90 +/- 5 days)
5 Effect of Home Exercise Activity on Cortisol and Depression in COPD Patients During the Pandemic COVID-19

exercise activity during the COVID pandemic is appreciated to be conducted in home especially for chronic chest diseases as chronic obstructive pulmonary disease (COPD) to reduce the chance of viral contamination during the COVID-19 pandemic.

NCT04639349
Conditions
  1. Chronic Obstructive Pulmonary Disease
Interventions
  1. Behavioral: exercise group
  2. Other: control group
MeSH:Lung Diseases, Obstructive Pulmonary Disease, Chronic Obstructive
HPO:Chronic pulmonary obstruction Pulmonary obstruction

Primary Outcomes

Description: it will be measured in plasma

Measure: cortisol

Time: It will be measured after eight weeks of training

Description: this a questionnaire that will assess anxiety and depression in COPD patients

Measure: hospital anxiety and depression scale

Time: It will be measured after eight weeks of training

Secondary Outcomes

Description: it will be a measurement for lung volume and capacities

Measure: pulmonary function test

Time: It will be measured after eight weeks of training

Description: It is an inflammatory marker in plasma

Measure: Interleukin-8

Time: It will be measured after eight weeks of training

Description: it will measure body mass changes

Measure: body mass index

Time: It will be measured after eight weeks of training

Description: it assess functional capacity

Measure: six minute walking test

Time: It will be measured after eight weeks of training

Description: It assess the effect of COPD on general quality of life

Measure: St. George's respiratory questionnaire

Time: It will be measured after eight weeks of training
6 Feasibility of Using a Home-Based High Frequency Chest Wall Oscillation Device (AffloVest) in At-Risk Respiratory Patients to Decrease Acute Respiratory Care Burden During the COVID-19 Pandemic

The purpose of the study is to investigate the addition of high frequency chest wall oscillation (HFCWO) therapy to the prescribed care regimen to support the diaphragm during airway clearance among post-COVID patients with COPD and chronic productive cough as a way to limit the advancement of pulmonary symptoms and need for critical services during recovery from COVID-19.

NCT04654481
Conditions
  1. Chronic Obstructive Pulmonary Disease
  2. Chronic Cough
  3. Covid19
Interventions
  1. Device: HCFWO
  2. Other: Standard Care Plus Monitoring
MeSH:Lung Diseases Lung Diseases, Obstructive Pulmonary Disease, Chronic Obstructive
HPO:Abnormal lung morphology Chronic pulmonary obstruction Pulmonary obstruction

Primary Outcomes

Description: Change in forced expiratory volume in one second (FEV1) as compared to baseline, measured by home spirometer.

Measure: Change in forced expiratory volume in one second (FEV1)

Time: Baseline and up to 90 Days

Description: Changes in oxygen saturation from baseline as measured by pulse oximeter. Normal oxygen range is 95 to 100 percent and low oxygen range is under 90 percent.

Measure: Change in Oxygen Saturation level

Time: Baseline and up to 90 Days

Description: Changes in basal temperature as measured by digital thermometer. Fever is indicated at 100.4 F (38 C) or higher.

Measure: Change in Presence of Fever

Time: Baseline and up to 90 Days

Secondary Outcomes

Description: CAP Symptom Questionnaire records how much the patient rated the bothersomeness of the symptom. Each item is scored as "0" (Patient did not have this symptom), "1" (Not at All) to "5" (Extremely). Full range scale from 0 to 90, higher score indicating patient experiencing more frequent or more severe symptoms.

Measure: Change in Presence of pneumonia symptoms via Community Acquired Pneumonia (CAP) Symptom Questionnaire

Time: Baseline and up to 90 Days

Description: The QOL-B is a disease-specific questionnaire that measures symptoms, functioning, and health-related quality of life relevant to patients with bronchiectasis. Scores are generated from 37 items that fall on 8 domains: Physical Functioning, Role Functioning, Vitality, Emotional Functioning, Social Functioning, Treatment Burden, Health Perceptions, and Respiratory Symptoms. All subscales and the full range scale are standardized to score from 0 to 100, with higher scores indicating better enjoyment and satisfaction with specific life domains.

Measure: Change in Quality of life via Quality of Life Questionnaire-Respiratory (QOL-B)

Time: Baseline and up to 90 Days

Description: The PHQ-8 is the depression module, which scores each of the eight DSM-IV criteria as "0" (not at all) to "3" (nearly every day). Full scale from 0-24, with higher score indicating more severe symptoms.

Measure: Change in Mental health screening via Personal Health Questionnaire Depression Scale (PHQ-8)

Time: Baseline and up to 90 Days

Description: The General Anxiety Disorder 7-item questionnaire (GAD-7) is a 7-item questionnaire that asks user to rank how often they have been bothered by seven problems over the past two weeks from "0" (not at all) to "3" (nearly every day). Full scale from 0-21, with higher score indicating more symptoms.

Measure: Change in Mental health screening via General Anxiety Disorder-7 (GAD-7)

Time: Baseline and up to 90 Days

Description: Eight questions that are specific to recent literature describing patients' experiences of symptoms during COVID. They are rated on a frequency scale from "never" to "always," using a 1-4 point scale. Full scale range from 8 to 32, with higher scores indicating more frequent symptoms.

Measure: Change in COVID Symptom Checklist

Time: Baseline and up to 90 Days

Description: Amount of time used per week in minutes

Measure: AffloVest Usage

Time: 90 Days
7 Evaluating the Comparative Effectiveness of Telemedicine in Primary Care: Learning From the COVID-19 Pandemic

Leveraging a natural experiment approach, the investigators will examine rapidly changing telemedicine and in-person models of care during and after the COVID-19 crisis to determine whether certain patients could safely choose to continue telemedicine or telemedicine-supplemented care, rather than return to in-person care.

NCT04684836
Conditions
  1. Asthma
  2. Chronic Obstructive Pulmonary Disease (COPD
  3. Congestive Heart Failure
  4. Diabetes
  5. Hypertension
Interventions
  1. Other: Exposure to telemedicine, after the onset of the pandemic
MeSH:Lung Diseases, Obstructive Pulmonary Disease, Chronic Obstructive Heart Failure
HPO:Abnormal left ventricular function Chronic pulmonary obstruction Congestive heart failure Pulmonary obstruction Right ventricular failure

Primary Outcomes

Description: Avoidable emergency department (ED) admissions will be obtained from claims data

Measure: Number of avoidable emergency department (ED) admissions

Time: 30 days after the exposure to one of the comparator arms of clinic-level telemedicine used

Description: Avoidable emergency department (ED) admissions will be obtained from claims data

Measure: Number of avoidable emergency department (ED) admissions

Time: 60 days after the exposure to one of the comparator arms of clinic-level telemedicine used

Description: Avoidable emergency department (ED) admissions will be obtained from claims data

Measure: Number of avoidable emergency department (ED) admissions

Time: 6 months after the exposure to one of the comparator arms of clinic-level telemedicine used

Description: Avoidable emergency department (ED) admissions will be obtained from claims data

Measure: Number of avoidable emergency department (ED) admissions

Time: 12 months after the exposure to one of the comparator arms of clinic-level telemedicine used

Description: Unplanned hospital admissions from the ED will be obtained from claims data

Measure: Number of unplanned hospital admissions from the ED

Time: 30 days after the exposure to one of the comparator arms of clinic-level telemedicine used

Description: Unplanned hospital admissions from the ED will be obtained from claims data

Measure: Number of unplanned hospital admissions from the ED

Time: 60 days after the exposure to one of the comparator arms of clinic-level telemedicine used

Description: Unplanned hospital admissions from the ED will be obtained from claims data

Measure: Number of unplanned hospital admissions from the ED

Time: 6 months after the exposure to one of the comparator arms of clinic-level telemedicine used

Description: Unplanned hospital admissions from the ED will be obtained from claims data

Measure: Number of unplanned hospital admissions from the ED

Time: 12 months the comparator arms of clinic-level telemedicine used

Description: Continuity of care will be measured using the Bice-Boxerman Continuity of Care Index. The Bice-Boxerman continuity of care (COC) index reflects the relative share of all of a patient's visits during the year that are billed by distinct providers and/or practices. The index ranges from 0 to 1, where 0 indicates that each visit involved a different provider than all other visits, and 1 that all visits were billed by a single provider, representing continuity of care.

Measure: Continuity of care as assessed by the Bice-Boxerman Continuity of Care Index

Time: 30 days after the exposure to one of the comparator arms of clinic-level telemedicine used

Description: Continuity of care will be measured using the Bice-Boxerman Continuity of Care Index. The Bice-Boxerman continuity of care (COC) index reflects the relative share of all of a patient's visits during the year that are billed by distinct providers and/or practices. The index ranges from 0 to 1, where 0 indicates that each visit involved a different provider than all other visits, and 1 that all visits were billed by a single provider, representing continuity of care.

Measure: Continuity of care as assessed by the Bice-Boxerman Continuity of Care Index

Time: 60 days after the exposure to one of the comparator arms of clinic-level telemedicine used

Description: Continuity of care will be measured using the Bice-Boxerman Continuity of Care Index. The Bice-Boxerman continuity of care (COC) index reflects the relative share of all of a patient's visits during the year that are billed by distinct providers and/or practices. The index ranges from 0 to 1, where 0 indicates that each visit involved a different provider than all other visits, and 1 that all visits were billed by a single provider, representing continuity of care.

Measure: Continuity of care as assessed by the Bice-Boxerman Continuity of Care Index

Time: 6 months after the exposure to one of the comparator arms of clinic-level telemedicine used

Description: Continuity of care will be measured using the Bice-Boxerman Continuity of Care Index. The Bice-Boxerman continuity of care (COC) index reflects the relative share of all of a patient's visits during the year that are billed by distinct providers and/or practices. The index ranges from 0 to 1, where 0 indicates that each visit involved a different provider than all other visits, and 1 that all visits were billed by a single provider, representing continuity of care.

Measure: Continuity of care as assessed by the Bice-Boxerman Continuity of Care Index

Time: 12 months after the exposure to one of the comparator arms of clinic-level telemedicine used

Description: Continuity of care as assessed by the Breslau Usual Provider of Care measure. The Breslau Usual Provider of Care index is also an indicator of continuity of care, ranging from 0 to 1, where 1 represents continuity of care.

Measure: Continuity of care as assessed by the Breslau Usual Provider of Care measure

Time: 30 days after the exposure to one of the comparator arms of clinic-level telemedicine used

Description: Continuity of care as assessed by the Breslau Usual Provider of Care measure. The Breslau Usual Provider of Care index is also an indicator of continuity of care, ranging from 0 to 1, where 1 represents continuity of care.

Measure: Continuity of care as assessed by the Breslau Usual Provider of Care measure

Time: 60 days after the exposure to one of the comparator arms of clinic-level telemedicine used

Description: Continuity of care as assessed by the Breslau Usual Provider of Care measure. The Breslau Usual Provider of Care index is also an indicator of continuity of care, ranging from 0 to 1, where 1 represents continuity of care.

Measure: Continuity of care as assessed by the Breslau Usual Provider of Care measure

Time: 6 months after the exposure to one of the comparator arms of clinic-level telemedicine used

Description: Continuity of care as assessed by the Breslau Usual Provider of Care measure. The Breslau Usual Provider of Care index is also an indicator of continuity of care, ranging from 0 to 1, where 1 represents continuity of care.

Measure: Continuity of care as assessed by the Breslau Usual Provider of Care measure

Time: 12 months after the exposure to one of the comparator arms of clinic-level telemedicine used

Description: Continuity of care as assessed by attendance at follow-up appointment.

Measure: Continuity of care as assessed by attendance at follow-up appointment

Time: 30 days after the exposure to one of the comparator arms of clinic-level telemedicine used

Description: Continuity of care as assessed by attendance at follow-up appointment.

Measure: Continuity of care as assessed by attendance at follow-up appointment

Time: 60 days after the exposure to one of the comparator arms of clinic-level telemedicine used

Description: Continuity of care as assessed by attendance at follow-up appointment.

Measure: Continuity of care as assessed by attendance at follow-up appointment

Time: 6 months after the exposure to one of the comparator arms of clinic-level telemedicine used

Description: Continuity of care as assessed by attendance at follow-up appointment.

Measure: Continuity of care as assessed by attendance at follow-up appointment

Time: 12 months after the exposure to one of the comparator arms of clinic-level telemedicine used

Secondary Outcomes

Description: Evidence of controlled disease as indicated by as indicated by the National Quality Forum (NQF 0059): Diabetes: Hemoglobin A1c (HbA1c) Poor Control (>9%), which is the percentage of patients 18 - 75 years of age with diabetes who had hemoglobin A1c > 9.0% during the measurement period

Measure: Evidence of controlled disease as indicated by as indicated by the National Quality Forum (NQF 0059): Diabetes: Hemoglobin A1c (HbA1c) Poor Control (>9%)

Time: 30 days after the exposure to one of the comparator arms of clinic-level telemedicine used

Description: Evidence of controlled disease as indicated by as indicated by the National Quality Forum (NQF 0059): Diabetes: Hemoglobin A1c (HbA1c) Poor Control (>9%), which is the percentage of patients 18 - 75 years of age with diabetes who had hemoglobin A1c > 9.0% during the measurement period

Measure: Evidence of controlled disease as indicated by as indicated by the National Quality Forum (NQF 0059): Diabetes: Hemoglobin A1c (HbA1c) Poor Control (>9%)

Time: 60 days after the exposure to one of the comparator arms of clinic-level telemedicine used

Description: Evidence of controlled disease as indicated by as indicated by the National Quality Forum (NQF 0059): Diabetes: Hemoglobin A1c (HbA1c) Poor Control (>9%), which is the percentage of patients 18 - 75 years of age with diabetes who had hemoglobin A1c > 9.0% during the measurement period

Measure: Evidence of controlled disease as indicated by as indicated by the National Quality Forum (NQF 0059): Diabetes: Hemoglobin A1c (HbA1c) Poor Control (>9%)

Time: 6 months after the exposure to one of the comparator arms of clinic-level telemedicine used

Description: Evidence of controlled disease as indicated by as indicated by the National Quality Forum (NQF 0059): Diabetes: Hemoglobin A1c (HbA1c) Poor Control (>9%), which is the percentage of patients 18 - 75 years of age with diabetes who had hemoglobin A1c > 9.0% during the measurement period

Measure: Evidence of controlled disease as indicated by as indicated by the National Quality Forum (NQF 0059): Diabetes: Hemoglobin A1c (HbA1c) Poor Control (>9%)

Time: 12 months after the exposure to one of the comparator arms of clinic-level telemedicine used

Description: Evidence of controlled disease as indicated by as indicated by the National Quality Forum (NQF 0018): Controlling High Blood Pressure, which is the percentage of patients 18 - 85 with hypertension diagnosis and adequate control (< 140/90 mmHg)

Measure: Evidence of controlled disease as indicated by as indicated by the National Quality Forum (NQF 0018): Controlling High Blood Pressure

Time: 30 days after the exposure to one of the comparator arms of clinic-level telemedicine used

Description: Evidence of controlled disease as indicated by as indicated by the National Quality Forum (NQF 0018): Controlling High Blood Pressure, which is the percentage of patients 18 - 85 with hypertension diagnosis and adequate control (< 140/90 mmHg)

Measure: Evidence of controlled disease as indicated by as indicated by the National Quality Forum (NQF 0018): Controlling High Blood Pressure

Time: 60 days after the exposure to one of the comparator arms of clinic-level telemedicine used

Description: Evidence of controlled disease as indicated by as indicated by the National Quality Forum (NQF 0018): Controlling High Blood Pressure, which is the percentage of patients 18 - 85 with hypertension diagnosis and adequate control (< 140/90 mmHg)

Measure: Evidence of controlled disease as indicated by as indicated by the National Quality Forum (NQF 0018): Controlling High Blood Pressure

Time: 6 months after the exposure to one of the comparator arms of clinic-level telemedicine used

Description: Evidence of controlled disease as indicated by as indicated by the National Quality Forum (NQF 0018): Controlling High Blood Pressure, which is the percentage of patients 18 - 85 with hypertension diagnosis and adequate control (< 140/90 mmHg)

Measure: Evidence of controlled disease as indicated by as indicated by the National Quality Forum (NQF 0018): Controlling High Blood Pressure

Time: 12 months after the exposure to one of the comparator arms of clinic-level telemedicine used

Description: Days per month not in hospital or institutional setting

Measure: Days at home

Time: 30 days after the exposure to one of the comparator arms of clinic-level telemedicine used

Description: Days per month not in hospital or institutional setting

Measure: Days at home

Time: 60 days after the exposure to one of the comparator arms of clinic-level telemedicine used

Description: Days per month not in hospital or institutional setting

Measure: Days at home

Time: 6 months after the exposure to one of the comparator arms of clinic-level telemedicine used

Description: Days per month not in hospital or institutional setting

Measure: Days at home

Time: 12 months after the exposure to one of the comparator arms of clinic-level telemedicine used

Description: Patient experiences based on the Patient Satisfaction Questionnaire (PSQ-18), which is a 5-scale questionnaire including questions on patient satisfaction, communication quality with providers and accessibility/convenience of care.

Measure: Patient experiences based on the Patient Satisfaction Questionnaire (PSQ-18)

Time: 12 months after the exposure to one of the comparator arms of clinic-level telemedicine used

Description: For individuals who accessed a telemedicine visit, we will ask questions based on the validated Telehealth Usability Questionnaire (TUQ), including the ease of use and access to the telemedicine service, quality of the interaction with the provider, and satisfaction

Measure: Ease of use and access to telemedicine based on Telehealth Usability Questionnaire (TUQ)

Time: 12 months after the exposure to one of the comparator arms of clinic-level telemedicine used

HPO Nodes


Reports

Data processed on January 01, 2021.

An HTML report was created for each of the unique drugs, MeSH, and HPO terms associated with COVID-19 clinical trials. Each report contains a list of either the drug, the MeSH terms, or the HPO terms. All of the terms in a category are displayed on the left-hand side of the report to enable easy navigation, and the reports contain a list of correlated drugs, MeSH, and HPO terms. Further, all reports contain the details of the clinical trials in which the term is referenced. Every clinical trial report shows the mapped HPO and MeSH terms, which are also hyperlinked. Related HPO terms, with their associated genes, protein mutations, and SNPs are also referenced in the report.

Drug Reports   MeSH Reports   HPO Reports  

Interventions

4,818 reports on interventions/drugs

MeSH

706 reports on MeSH terms

HPO

306 reports on HPO terms

All Terms

Alphabetical index of all Terms

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