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Clinical Trials/NCT04539756
NCT04539756
Completed
N/A

Does an Online Two-week Positive Psychological Intervention Improve Positive Affect in Young Adults?

University of Pittsburgh1 site in 1 country250 target enrollmentSeptember 8, 2020
ConditionsHealthy

Overview

Phase
N/A
Intervention
Not specified
Conditions
Healthy
Sponsor
University of Pittsburgh
Enrollment
250
Locations
1
Primary Endpoint
Change from baseline in positive affect at 1 week post-intervention
Status
Completed
Last Updated
4 years ago

Overview

Brief 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.

Registry
clinicaltrials.gov
Start Date
September 8, 2020
End Date
November 20, 2020
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Caitlin M. DuPont

Principal Investigator

University of Pittsburgh

Eligibility Criteria

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.

Outcomes

Primary Outcomes

Change from baseline in positive affect at 1 week post-intervention

Time Frame: Assessed twice, once before the intervention and a second time within one week of completing the 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.

Secondary Outcomes

  • Change from baseline in psychological well-being at 1 week post-intervention(Assessed twice, once before the intervention and a second time within one week of completing the intervention.)
  • Change from baseline in light physical activity (in general) at 1 week post-intervention(Assessed twice, once before the intervention and a second time within one week of completing the intervention.)
  • Change from baseline in optimism at 1 week post-intervention(Assessed twice, once before the intervention and a second time within one week of completing the intervention.)
  • Change from baseline in perceived stress at 1 week post-intervention(Assessed twice, once before the intervention and a second time within one week of completing the intervention.)
  • Change from baseline in life satisfaction at 1 week post-intervention(Assessed twice, once before the intervention and a second time within one week of completing the intervention.)
  • Change from baseline in loneliness at 1 week post-intervention(Assessed twice, once before the intervention and a second time within one week of completing the intervention.)
  • Change from baseline in depressive symptoms at 1 week post-intervention(Assessed twice, once before the intervention and a second time within one week of completing the intervention.)
  • Change from baseline in anxiety symptoms at 1 week post-intervention(Assessed twice, once before the intervention and a second time within one week of completing the intervention.)
  • Change from baseline in sleep quality (in general) at 1 week post-intervention(Assessed twice, once before the intervention and a second time within one week of completing the intervention.)
  • Change from baseline in perceived social support at 1 week post-intervention(Assessed twice, once before the intervention and a second time within one week of completing the intervention.)
  • Change from baseline in moderate physical activity (in general) at 1 week post-intervention(Assessed twice, once before the intervention and a second time within one week of completing the intervention.)
  • Change from baseline in negative affect at 1 week post-intervention(Assessed twice, once before the intervention and a second time within one week of completing the intervention.)
  • Change from baseline in sleep quantity (in general) at 1 week post-intervention(Assessed twice, once before the intervention and a second time within one week of completing the intervention.)

Study Sites (1)

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