Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04539756
Other study ID # STUDY20060287
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 8, 2020
Est. completion date November 20, 2020

Study information

Verified date July 2021
Source University of Pittsburgh
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Completed
Enrollment 250
Est. completion date November 20, 2020
Est. primary completion date November 20, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Must be an undergraduate student at the University of Pittsburgh that is currently taking Introduction to Psychology. - Must be at least 18 years old - Not currently prescribed medications for cardiac arrythmias - Report no history of heart surgery, heart attack, or stroke - Not currently pregnant - Must deny having current symptoms consistent with COVID-19. Exclusion Criteria: - If the participant does not meet the inclusion criteria.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
positive psychological intervention
Participants will be asked to complete writing activities every other day. They will choose which activity they would like to complete each day, from a menu of six different activities. Each activity is a different positive psychology exercise.
Active control condition
Participants will be asked to complete the same writing activity each day, which will ask them to list their daily activities. Participants will be encouraged to process their daily activities superficially by the receiving the following instructions: (1) list each activity in brief, incomplete sentences, (2) document only facts about performing the activities, and (3) to not provide any information about emotional responses to performing the activities. By following these instructions, participants are presumably deriving less meaning from their activities, which may minimize gains in positive affect in the active control condition

Locations

Country Name City State
United States University of Pittsburgh Pittsburgh Pennsylvania

Sponsors (1)

Lead Sponsor Collaborator
University of Pittsburgh

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Other Loneliness 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. Assessed every other day, after participants complete each activity for up to 2 weeks.
Other Connectedness 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. Assessed every other day, after participants complete each activity for up to 2 weeks.
Other Stress 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. Assessed every other day, after participants complete each activity for up to 2 weeks.
Other School-specific stress 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. Assessed every other day, after participants complete each activity for up to 2 weeks.
Other Light physical activity (today) Participants will self-report minutes of light physical activity that they completed that day. Larger numbers reflect better outcomes. Assessed every other day, after participants complete each activity for up to 2 weeks.
Other Moderate to vigorous physical activity (today) Participants will self-report minutes of moderate to vigorous physical activity that they completed that day. Larger numbers reflect better outcomes. Assessed every other day, after participants complete each activity for up to 2 weeks.
Other Sleep quantity (today) 1-items asking participants to report how long they slept the night before. Assessed every other day, after participants complete each activity for up to 2 weeks.
Other Sleep quality (today) 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. Assessed every other day, after participants complete each activity for up to 2 weeks.
Primary Change from baseline in positive affect at 1 week post-intervention 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. Assessed twice, once before the intervention and a second time within one week of completing the intervention.
Primary Change from baseline in positive affect at 1 week post-intervention 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. Assessed twice, once before the intervention and a second time within one week of completing the intervention.
Secondary Change from baseline in optimism at 1 week post-intervention 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. Assessed twice, once before the intervention and a second time within one week of completing the intervention.
Secondary Change from baseline in life satisfaction at 1 week post-intervention 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. Assessed twice, once before the intervention and a second time within one week of completing the intervention.
Secondary Change from baseline in psychological well-being at 1 week post-intervention 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. Assessed twice, once before the intervention and a second time within one week of completing the intervention.
Secondary Change from baseline in perceived stress at 1 week post-intervention 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. Assessed twice, once before the intervention and a second time within one week of completing the intervention.
Secondary Change from baseline in perceived social support at 1 week post-intervention 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. Assessed twice, once before the intervention and a second time within one week of completing the intervention.
Secondary Change from baseline in loneliness at 1 week post-intervention 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. Assessed twice, once before the intervention and a second time within one week of completing the intervention.
Secondary Change from baseline in depressive symptoms at 1 week post-intervention 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. Assessed twice, once before the intervention and a second time within one week of completing the intervention.
Secondary Change from baseline in anxiety symptoms at 1 week post-intervention 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. Assessed twice, once before the intervention and a second time within one week of completing the intervention.
Secondary Change from baseline in light physical activity (in general) at 1 week post-intervention 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. Assessed twice, once before the intervention and a second time within one week of completing the intervention.
Secondary Change from baseline in moderate physical activity (in general) at 1 week post-intervention 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. Assessed twice, once before the intervention and a second time within one week of completing the intervention.
Secondary Change from baseline in sleep quality (in general) at 1 week post-intervention 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. Assessed twice, once before the intervention and a second time within one week of completing the intervention.
Secondary Change from baseline in sleep quantity (in general) at 1 week post-intervention 1-items asking participants to report how long they typically sleep each night. Assessed twice, once before the intervention and a second time within one week of completing the intervention.
Secondary Change from baseline in negative affect at 1 week post-intervention 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. Assessed twice, once before the intervention and a second time within one week of completing the intervention.
Secondary Change from baseline in negative affect at 1 week post-intervention 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. Assessed twice, once before the intervention and a second time within one week of completing the intervention.
See also
  Status Clinical Trial Phase
Recruiting NCT06052553 - A Study of TopSpin360 Training Device N/A
Completed NCT05511077 - Biomarkers of Oat Product Intake: The BiOAT Marker Study N/A
Recruiting NCT04632485 - Early Detection of Vascular Dysfunction Using Biomarkers From Lagrangian Carotid Strain Imaging
Completed NCT05931237 - Cranberry Flavan-3-ols Consumption and Gut Microbiota in Healthy Adults N/A
Completed NCT04527718 - Study of the Safety, Tolerability and Pharmacokinetics of 611 in Adult Healthy Volunteers Phase 1
Terminated NCT04556032 - Effects of Ergothioneine on Cognition, Mood, and Sleep in Healthy Adult Men and Women N/A
Completed NCT04065295 - A Study to Test How Well Healthy Men Tolerate Different Doses of BI 1356225 Phase 1
Completed NCT04107441 - AX-8 Drug Safety, Tolerability and Plasma Levels in Healthy Subjects Phase 1
Completed NCT04998695 - Health Effects of Consuming Olive Pomace Oil N/A
Completed NCT01442831 - Evaluate the Absorption, Metabolism, And Excretion Of Orally Administered [14C] TR 701 In Healthy Adult Male Subjects Phase 1
Terminated NCT05934942 - A Study in Healthy Women to Test Whether BI 1358894 Influences the Amount of a Contraceptive in the Blood Phase 1
Recruiting NCT05525845 - Studying the Hedonic and Homeostatic Regulation of Food Intake Using Functional MRI N/A
Completed NCT05515328 - A Study in Healthy Men to Test How BI 685509 is Processed in the Body Phase 1
Completed NCT05030857 - Drug-drug Interaction and Food-effect Study With GLPG4716 and Midazolam in Healthy Subjects Phase 1
Completed NCT04967157 - Cognitive Effects of Citicoline on Attention in Healthy Men and Women N/A
Recruiting NCT04714294 - Evaluate the Safety, Tolerability and Pharmacokinetics Characteristics of HPP737 in Healthy Volunteers Phase 1
Recruiting NCT04494269 - A Study to Evaluate Pharmacokinetics and Safety of Tegoprazan in Subjects With Hepatic Impairment and Healthy Controls Phase 1
Recruiting NCT04098510 - Concentration of MitoQ in Human Skeletal Muscle N/A
Completed NCT03308110 - Bioavailability and Food Effect Study of Two Formulations of PF-06650833 Phase 1
Completed NCT04052711 - A Randomized, Controlled Study to Evaluate the Sensitizing Potential of FMX-101 in Healthy Volunteers Using a Repeat Insult Patch Test Design Phase 1