CovidResearchTrials by Shray Alag


CovidResearchTrials Covid 19 Research using Clinical Trials (Home Page)


ObservationWiki

Developed by Shray Alag
Clinical Trial MeSH HPO Drug Gene SNP Protein Mutation


Correlated Drug Terms (1)


Name (Synonyms) Correlation
drug1149 IMM-101 Wiki 0.71

Correlated MeSH Terms (2)


Name (Synonyms) Correlation
D020521 Stroke NIH 0.22
D007239 Infection NIH 0.04

Correlated HPO Terms (1)


Name (Synonyms) Correlation
HP:0001297 Stroke HPO 0.22

There are 2 clinical trials

Clinical Trials


1 Stroke Rehabilitation Outcome During COVID-19 Lockdown

COVID-19 has a big impact on individuals and society as a whole. Especially persons with (multiple) comorbidities such as stroke are affected. The impact of COVID-19 on stroke rehabilitation delivery and stroke patients' functioning is unclear.

NCT04373109 Stroke Rehabilitation COVID-19 Cohort Studies Behavioral: Observation
MeSH:Stroke
HPO:Stroke

Primary Outcomes

Description: Nature of rehabilitation therapy, and number and duration of rehabilitation therapy sessions

Measure: Rehabilitation data

Time: 3 month after start lockdown

Description: Patient-reported upper limb use in daily life

Measure: Motor Activity Log - 14 Item Version

Time: 3 month after start lockdown

Description: Patient-reported engagement in physical activity in daily life

Measure: International Physical Activity Questionnaire

Time: 3 month after start lockdown

Description: Patient-self-assessment comprising the following categories: 1) physical function, 2) anxiety, 3) depression, 4) fatigue, 5) sleep disturbance, 6) ability to participate in social roles and activities, 7) pain interference and 8) pain intensity

Measure: Patient-Reported Outcomes Measurement Information System - 29 Version

Time: 3 month after start lockdown

Secondary Outcomes

Description: Patient-reported global rating of physical activity engagement and upper limb use in daily life

Measure: Global Rating of Perceived Changes (physical activity engagement and upper limb use)

Time: 4 weeks after lockdown ("extraordinary situation" as defined by the Swiss law), 3 months after lockdown, 6 months after lockdown

Description: Self-reported questionnaire regarding severity of fatigue and its influence on the performance of daily life activities

Measure: Fatigue Severity Scale

Time: 4 weeks after lockdown ("extraordinary situation" as defined by the Swiss law), 3 months after lockdown, 6 months after lockdown

Description: Depression and anxiety

Measure: Hospital Anxiety and Depression Scale

Time: 4 weeks after lockdown ("extraordinary situation" as defined by the Swiss law), 3 months after lockdown, 6 months after lockdown

Description: Assesses cognitive functions

Measure: Montreal Cognitive Assessment

Time: 4 weeks after lockdown ("extraordinary situation" as defined by the Swiss law), 3 months after lockdown, 6 months after lockdown

Description: Classification regarding the ability to walk independently, with or without a walking aid and takes the type of walking surface into account

Measure: Functional Ambulation Categories

Time: 4 weeks after lockdown ("extraordinary situation" as defined by the Swiss law), 3 months after lockdown, 6 months after lockdown

Description: Gait speed and cadence

Measure: Ten-Meter Walk Test

Time: 4 weeks after lockdown ("extraordinary situation" as defined by the Swiss law), 3 months after lockdown, 6 months after lockdown

Description: Measures the ability of patients to make postural adjustments (e.g, move in bed), transfer (e.g. be-tween bed to chair), walk, and use stairs

Measure: Rivermead Mobility Index

Time: 4 weeks after lockdown ("extraordinary situation" as defined by the Swiss law), 3 months after lockdown, 6 months after lockdown

Description: Self-reported measure in which patients rate how confident they are in maintaining balance when performing 16 daily life tasks

Measure: Activities-specific Balance Confidence Scale

Time: 4 weeks after lockdown ("extraordinary situation" as defined by the Swiss law), 3 months after lockdown, 6 months after lockdown

Description: Upper and lower limb motor function

Measure: Fugl-Meyer Motor Assessment

Time: 4 weeks after lockdown ("extraordinary situation" as defined by the Swiss law), 3 months after lockdown, 6 months after lockdown

Description: Upper limb capacity

Measure: Action Research Arm Test

Time: 4 weeks after lockdown ("extraordinary situation" as defined by the Swiss law), 3 months after lockdown, 6 months after lockdown

Description: Global disability

Measure: modified Rankin Scale

Time: 4 weeks after lockdown ("extraordinary situation" as defined by the Swiss law), 3 months after lockdown, 6 months after lockdown

Description: Neurological impairments

Measure: National Institutes of Health Stroke Scale

Time: 4 weeks after lockdown ("extraordinary situation" as defined by the Swiss law), 3 months after lockdown, 6 months after lockdown

Description: Nature of rehabilitation therapy, and number and duration of rehabilitation therapy sessions

Measure: Rehabilitation data

Time: 4 weeks after lockdown ("extraordinary situation" as defined by the Swiss law), 6 months after lockdown

Description: Patient-reported upper limb use in daily life

Measure: Motor Activity Log - 14 Item Version

Time: 4 weeks after lockdown ("extraordinary situation" as defined by the Swiss law), 6 months after lockdown

Description: Patient-reported engagement in physical activity in daily life

Measure: International Physical Activity Questionnaire

Time: 4 weeks after lockdown ("extraordinary situation" as defined by the Swiss law), 6 months after lockdown

Description: Patient-self-assessment comprising the following categories: 1) physical function, 2) anxiety, 3) depression, 4) fatigue, 5) sleep disturbance, 6) ability to participate in social roles and activities, 7) pain interference and 8) pain intensity

Measure: Patient-Reported Outcomes Measurement Information System - 29 Version

Time: 4 weeks after lockdown ("extraordinary situation" as defined by the Swiss law), 6 months after lockdown

2 COV-IMMUNO: A Randomized, Phase III Trial of Immunization With IMM-101 Versus Observation for the Prevention of Severe Respiratory and COVID-19 Related Infections in Cancer Patients at Increased Risk of Exposure

The purpose of this study is to find out if immunization with IMM-101 will reduce the incidence of severe respiratory and COVID-19 infections in cancer patients.

NCT04442048 Cancer Covid-19 Biological: IMM-101 Other: Observation
MeSH:Infection

Primary Outcomes

Description: WHO definition of "influenza-like illness" (ILI) [Fitzner 2018] or confirmed viral/bacterial respiratory infection AND Results in a change or delay in cancer treatment or requirement for and unscheduled medical assesment, hospitalization or death.

Measure: The rate of "flu-like illness" which includes:

Time: 1 year

Secondary Outcomes

Measure: The incidence of documented COVID-19 infection (confirmed by any Health Canada approved COVID-19 test. Both symptomatic and asymptomatic infections will be documented

Time: 1 year

Measure: The rate of severe respiratory and COVID-19 infection defined as a confirmed COVID-19 infection leading to hospitalization, ICU admission or death

Time: 1 year

Measure: The number of events that meet the definition of the primary endpoint, as measured within the one-year follow-up (patients may meet the primary endpoint more than once and be counted multiple times).

Time: 1 year

Measure: The incidence of COVID-19 seroconverted patients between baseline, 3 months, 6 months and 12 months

Time: 3, 6, and 12 months

Measure: The incremental cost-effectiveness ratio (in the unit of CAD$ per life-years gained) measured with EQ-5D-5L

Time: 1 year

Measure: Failure-free survival, as time from enrollment to recurrence or progression declared by the investigator on the basis of objective standard evaluation consistent with the disease site or death

Time: 1 year

Measure: Overall survival (OS), as time from enrollment to death from any cause

Time: 1 year

Measure: Incidence, frequency, and severity of AEs considered possibly, probably or definitely related to receipt of IMM-101

Time: 1 year

Measure: Incidence and frequency of local injection site reactions subsequent to IMM-101 administration

Time: 1 year

Measure: Incidence and duration of ICU admission related to documented COVID-19 infection

Time: 1 year


Related HPO nodes (Using clinical trials)