Developed by Shray Alag, The Harker School
Sections: Correlations,
Clinical Trials, and HPO
Navigate: Clinical Trials and HPO
| Name (Synonyms) | Correlation | |
|---|---|---|
| drug206 | Active control condition Wiki | 1.00 |
| drug1296 | ECCO2R Wiki | 1.00 |
| Name (Synonyms) | Correlation | |
|---|---|---|
| D012127 | Respiratory Distress Syndrome, Newborn NIH | 0.08 |
| D055371 | Acute Lung Injury NIH | 0.08 |
| D012128 | Respiratory Distress Syndrome, Adult NIH | 0.07 |
| Name (Synonyms) | Correlation |
|---|
Navigate: Correlations HPO
There is one clinical trial.
The current study aims to test whether an online two-week positive psychological intervention can increase positive affect in college students. Participants will be recruited from the University of Pittsburgh undergraduate subject pool. Students will be ineligible if they are under the age of 18; currently prescribed medications for cardiac arrythmias; have a history of heart surgery, heart attack, or stroke; are currently pregnant; or currently have symptoms consistent with COVID-19. This study includes an active control arm and an intervention arm. Both arms will be required to complete writing activities every other day for two weeks. Participants in the control arm will list their daily activities, while participants in the intervention arm will complete various positive psychology activities. Questionnaires assessing mood, emotional well-being, social functioning and a few health behaviors will be administered pre- and post-intervention. The investigators aim to recruit 250 undergraduate students with the hope that at least 50 participants per group will complete the entire study.
Description: Positive and Negative Affective Schedule (20-item). The possible range for this questionnaire is from 5 - 50. Baseline values will be subtracted from post-intervention values and a higher score on this measure represents a better outcome.
Measure: Change from baseline in positive affect at 1 week post-intervention Time: Assessed twice, once before the intervention and a second time within one week of completing the intervention.Description: Positive Emotional Style Questionnaire. The possible range for this questionnaire is from 0 - 36. Baseline values will be subtracted from post-intervention values and a higher score on this measure represents a better outcome.
Measure: Change from baseline in positive affect at 1 week post-intervention Time: Assessed twice, once before the intervention and a second time within one week of completing the intervention.Description: Life Orientation Test-Revised. The possible range for this questionnaire is from 6 - 30. Baseline values will be subtracted from post-intervention values and a higher score on this measure represents a better outcome.
Measure: Change from baseline in optimism at 1 week post-intervention Time: Assessed twice, once before the intervention and a second time within one week of completing the intervention.Description: PROMIS - General Life Satisfaction. The possible range for this questionnaire is from 10 - 70. Baseline values will be subtracted from post-intervention values and a higher score on this measure represents a better outcome.
Measure: Change from baseline in life satisfaction at 1 week post-intervention Time: Assessed twice, once before the intervention and a second time within one week of completing the intervention.Description: Psychological Well-Being Scale. The possible range for this questionnaire is from 42 - 294. Baseline values will be subtracted from post-intervention values and a higher score on this measure represents a better outcome.
Measure: Change from baseline in psychological well-being at 1 week post-intervention Time: Assessed twice, once before the intervention and a second time within one week of completing the intervention.Description: Perceived Stress Scale. The possible range for this questionnaire is from 0 - 40. Baseline values will be subtracted from post-intervention values and a higher score on this measure represents a worse outcome.
Measure: Change from baseline in perceived stress at 1 week post-intervention Time: Assessed twice, once before the intervention and a second time within one week of completing the intervention.Description: ISEL (12-item). The possible range for this questionnaire is from 12 - 48. Baseline values will be subtracted from post-intervention values and a higher score on this measure represents a better outcome.
Measure: Change from baseline in perceived social support at 1 week post-intervention Time: Assessed twice, once before the intervention and a second time within one week of completing the intervention.Description: UCLA Loneliness Scale (8-item). The possible range for this questionnaire is from 0 - 24. Baseline values will be subtracted from post-intervention values and a higher score on this measure represents a worse outcome.
Measure: Change from baseline in loneliness at 1 week post-intervention Time: Assessed twice, once before the intervention and a second time within one week of completing the intervention.Description: PROMIS - Emotional Distress - Depression - Short Form. The possible range for this questionnaire is from 8 - 40. Baseline values will be subtracted from post-intervention values and a higher score on this measure represents a worse outcome.
Measure: Change from baseline in depressive symptoms at 1 week post-intervention Time: Assessed twice, once before the intervention and a second time within one week of completing the intervention.Description: PROMIS - Emotional Distress - Anxiety - Short Form. The possible range for this questionnaire is from 7 - 35. Baseline values will be subtracted from post-intervention values and a higher score on this measure represents a worse outcome.
Measure: Change from baseline in anxiety symptoms at 1 week post-intervention Time: Assessed twice, once before the intervention and a second time within one week of completing the intervention.Description: 1-items asking participants to report minutes of light physical activity that they perform 'in general.' Baseline values will be subtracted from post-intervention values and a higher number on this measure represents a better outcome.
Measure: Change from baseline in light physical activity (in general) at 1 week post-intervention Time: Assessed twice, once before the intervention and a second time within one week of completing the intervention.Description: 1-item asking participants to report minutes of moderate to vigorous physical activity that they perform 'in general.' Baseline values will be subtracted from post-intervention values and a higher number on this measure represents a better outcome.
Measure: Change from baseline in moderate physical activity (in general) at 1 week post-intervention Time: Assessed twice, once before the intervention and a second time within one week of completing the intervention.Description: 1-item asking participants to report their overall sleep quality in general. Sleep quality was assessed on a Likert scale from Very bad (0) to Very good (5). Higher scores reflect a better outcome.
Measure: Change from baseline in sleep quality (in general) at 1 week post-intervention Time: Assessed twice, once before the intervention and a second time within one week of completing the intervention.Description: 1-items asking participants to report how long they typically sleep each night.
Measure: Change from baseline in sleep quantity (in general) at 1 week post-intervention Time: Assessed twice, once before the intervention and a second time within one week of completing the intervention.Description: Positive and Negative Affective Schedule. The possible range for this questionnaire is from 5 - 50. Baseline values will be subtracted from post-intervention values and a higher score on this measure represents a better outcome.
Measure: Change from baseline in negative affect at 1 week post-intervention Time: Assessed twice, once before the intervention and a second time within one week of completing the intervention.Description: Negative Emotional Style Questionnaires. The possible range for this questionnaire is from 0 - 36. Baseline values will be subtracted from post-intervention values and a higher score on this measure represents a worse outcome.
Measure: Change from baseline in negative affect at 1 week post-intervention Time: Assessed twice, once before the intervention and a second time within one week of completing the intervention.Description: Participants will be asked to rate how much they agree with the following statement on a visual analogue scale from "Not at all accurate (0)" to "Extremely Accurate (100)". The statements states: Today I feel lonely or isolated. Higher scores reflect worse outcomes.
Measure: Loneliness Time: Assessed every other day, after participants complete each activity for up to 2 weeks.Description: Participants will be asked to rate how much they agree with the following statement on a visual analogue scale from "Not at all accurate (0)" to "Extremely Accurate (100)". The statements states: Today I feel connected to others. Higher scores reflect better outcomes.
Measure: Connectedness Time: Assessed every other day, after participants complete each activity for up to 2 weeks.Description: Participants will be asked to rate how much they agree with the following statements on a visual analogue scale from "Not at all accurate (0)" to "Extremely Accurate (100)". Stress will be assessed by the one-item statement: 'Today I feel stressed.' Higher scores reflect worse outcomes.
Measure: Stress Time: Assessed every other day, after participants complete each activity for up to 2 weeks.Description: Participants will be asked to rate how much they agree with the following statements on a visual analogue scale from "Not at all accurate (0)" to "Extremely Accurate (100)". School stress will be assessed by the one-item statement: 'Today I feel nervous or overwhelmed about school.' Higher scores reflect worse outcomes.
Measure: School-specific stress Time: Assessed every other day, after participants complete each activity for up to 2 weeks.Description: Participants will self-report minutes of light physical activity that they completed that day. Larger numbers reflect better outcomes.
Measure: Light physical activity (today) Time: Assessed every other day, after participants complete each activity for up to 2 weeks.Description: Participants will self-report minutes of moderate to vigorous physical activity that they completed that day. Larger numbers reflect better outcomes.
Measure: Moderate to vigorous physical activity (today) Time: Assessed every other day, after participants complete each activity for up to 2 weeks.Description: 1-items asking participants to report how long they slept the night before.
Measure: Sleep quantity (today) Time: Assessed every other day, after participants complete each activity for up to 2 weeks.Description: Sleep quality was assessed on a 1-item Likert scale asking participants to rate their subjective sleep quality from Very bad (0) to Very good (5). Larger numbers represent better outcomes.
Measure: Sleep quality (today) Time: Assessed every other day, after participants complete each activity for up to 2 weeks.Alphabetical listing of all HPO terms. Navigate: Correlations Clinical Trials
Data processed on September 26, 2020.
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