Viewing Study NCT06483568



Ignite Creation Date: 2024-07-17 @ 12:02 PM
Last Modification Date: 2024-10-26 @ 3:33 PM
Study NCT ID: NCT06483568
Status: NOT_YET_RECRUITING
Last Update Posted: 2024-07-03
First Post: 2024-04-26

Brief Title: Behavioral Mechanisms and Health Outcomes of Positive Psychological Intervention
Sponsor: Rutgers The State University of New Jersey
Organization: Rutgers The State University of New Jersey

Study Overview

Official Title: Behavioral Mechanisms and Health Outcomes of Positive Psychological Intervention
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-06
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The goal of this clinical trial is to learn if engaging in a multi-activity positive psychology intervention increases emotional well-being

The main aims of this project are to

1 Test the efficacy of a multi-activity positive psychology intervention for increasing emotional well-being in a racial-ethnically and socioeconomically diverse sample
2 Identify physical and social behavioral mechanisms driving positive psychology intervention effects on emotional well-being change and the durability of these effects over time
3 Examine physical health outcomes stemming from emotional well-being gains

Participants will

Visit the laboratory three times to complete survey measures and physical assessments

Complete brief survey items three times a day for 10 weeks of the study period Engage with assigned activities weekly for four weeks of the study period
Detailed Description: Participation will span 20 weeks around a four-week treatment phase Assessments will involve three lab visits and experience sampling method surveys completed on participants smart phones in response to short message service SMS message alerts

Lab Visit 1 Baseline Participants will begin participation with an in-person lab visit held in small groups This visit will begin with a guided informed consent procedure Participants will complete baseline self-report measures and physiological assessments and receive procedure instructions

Pre-Intervention Monitoring weeks 1 2 For two weeks participants will compete three very brief experience sampling surveys per day

Random Assignment Treatment and Monitoring weeks 345 6 Participants will be randomly assigned to the online four-week Pathways to Happiness treatment condition or a matched activity control condition All participants will complete the four weeks of activities either Pathways to Happiness Positive Psychology Intervention PPI or control activities on the Pathways to Happiness platform They will complete weekly check-in items on the Pathways to Happiness platform to assess their compliance with the activity instructions and their experiences with the activities Participants in both conditions will continue completing experience sampling surveys during this time

Lab Visit 2 Post-Test after week 6 The second lab visit will occur after week six following the treatment phase It will involve identical questionnaires and physiological screenings as in the baseline visit

Post-Intervention Monitoring weeks 78 After the treatment phase two weeks of post-intervention experience sampling survey monitoring will begin

Waiting Period Participants will not engage in any formal study activities from weeks 9 to 19

Follow-Up Monitoring weeks 19-20 Follow-up experience sampling monitoring will commence for the final two weeks of the study 10 weeks after the previous monitoring period

Lab Visit 3 Follow-Up after week 20 The final lab visit identical to the others will occur after week 20 and will conclude with an exit interview regarding participants experiences in the study and with each PPI activity

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None