- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05267132
Adolescent Acts of Kindness Intervention With Reflection
November 29, 2023 updated by: Andrew J. Fuligni, PhD, University of California, Los Angeles
Adolescents will complete a 4-week intervention, during which they will either complete a kind act for others, complete a kind act for others with a reflection component, or report their daily activities three days per week.
Psychological measures will be indexed before and after the intervention.
Study Overview
Status
Recruiting
Conditions
Detailed Description
There is growing policy and scientific interest in promoting the positive benefits of kindness and prosociality.
This is particularly true for adolescents, whose psychological and social maturation offers fertile ground in which kindness can be seeded early in life with potentially positive effects on their psychological health.
Much of the existing efforts have focused on large-scale community engagement and service-learning programs.
Investigating less costly and time-intensive alternatives is necessary to broaden engagement and access.
This project aims to implement one such effort with an enhanced acts of kindness intervention for adolescents.
The enhancement incorporates existing evidence that requiring adolescents to reflect upon and savor their experience of helping others promotes the positive impact of such interventions.
120 high-school-aged youth will be recruited and assigned to one of three groups (40/group).
Participants will either conduct a kind act for others, complete a kind act for others with a reflection component (enhanced condition), or report their daily activities three days per week for 4 weeks.
During this intervention, they will receive text messages 3 days per week instructing them to complete their respective act.
Participants will provide a brief description of this act that evening, as well as complete brief surveys at the end of the week for each week of the intervention.
Participants will also complete a pre- and post-intervention questionnaire and participants' parents will complete a brief survey at the start of the study to provide demographic information and an idea of what prosocial behaviors participants witnessed in their home.
The investigators will use these data to assess the effects of prosocial behavior on psychological health.
Conceptual frameworks from developmental psychology guide the hypothesis that prosocial behavior will influence adolescents.
Study Type
Interventional
Enrollment (Estimated)
120
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Xochitl A Smola, MA
- Phone Number: 310-794-5104
- Email: xsmola16@ucla.edu
Study Locations
-
-
California
-
Los Angeles, California, United States, 90066
- Recruiting
- Adolescent Development Lab
-
Contact:
- Andrew J Fuligni, PhD
- Phone Number: 310-794-6033
- Email: afuligni@ucla.edu
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
14 years to 17 years (Child)
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Between the ages of 14-17
Exclusion Criteria:
- None
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Kindness to Others with Reflection
Participants will complete the 'Other-Focused Acts of Kindness Intervention' by performing acts of kindness for others and will also complete a reflection component.
They will be asked to complete 3 kind acts for others throughout the week for 4 weeks.
They will receive text messages three days per week (either Tuesday, Thursday, and Saturday or Wednesday, Friday, and Sunday) and will report on their kind act later that day.
At the end of each intervention week, they will be asked to reflect upon their experience of performing kind acts for others.
|
Participants engage in positive behaviors by completing acts of kindness for others three times per week.
These acts should require effort and be outside of an individual's normal routine.
Participants will then reflect on their kind acts after each week.
|
Active Comparator: Kindness to Others
Participants will complete the 'Other-Focused Acts of Kindness Intervention' by performing acts of kindness for others.
They will be asked to complete 3 kind acts for others throughout the week for 4 weeks.
They will receive text messages three days per week (either Tuesday, Thursday, and Saturday or Wednesday, Friday, and Sunday) and will report on their kind act later that day.
|
Participants engage in positive behaviors by completing acts of kindness for others three times per week.
These acts should require effort and be outside of an individual's normal routine.
|
Sham Comparator: Daily Report
Participants will complete the 'Daily Reports' and be asked to report their daily activities throughout the week for 4 weeks.
They will receive text messages three days per week (either Tuesday, Thursday, and Saturday or Wednesday, Friday, and Sunday) and will list activities from their day.
|
Participants will report their daily activities three times per week.
Aside from reporting at the end of the day, no changes should be made to the individual's normal routine.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Average Positive Affect
Time Frame: Weekly over 5 weeks
|
Average Positive Affect as assessed by the positive affect subscale of the Affect Adjective Checklist.
An average is taken across four items, and scores range from 1 to 5 with higher scores indicating more positive affect over the week.
|
Weekly over 5 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Average Psychological Flourishing
Time Frame: Baseline and one-week post intervention (elapsed time of 5 weeks)
|
Change in average psychological flourishing from baseline to one week following the intervention as assessed by Mental Health Continuum-Short Form at week 5.
An average is taken across 20 items, and scores range from 1 to 6, with higher values representing greater psychological flourishing.
|
Baseline and one-week post intervention (elapsed time of 5 weeks)
|
Average Negative Affect
Time Frame: Weekly over 5 weeks
|
Average negative affect as assessed by the negative affect subscale of the Affect Adjective Checklist.
An average is taken across five items, and scores range from 1 to 5 with higher scores indicating more negative affect over the week.
|
Weekly over 5 weeks
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Average Stress
Time Frame: Weekly over 5 weeks
|
Average stress as assessed by the Perceived Stress Scale.
An average is taken across 10 items, and scores range from 1 to 5 with higher scores indicating greater stress.
|
Weekly over 5 weeks
|
Sleep Quality
Time Frame: Weekly over 5 weeks
|
Sleep quality as assessed by the Pittsburgh Sleep Quality Index (PSQI).
The assessment has 7 components, each scored from 0 to 3. A sum is taken across these components, such that total scores range from 0 to 21 with higher scores indicating poorer sleep.
|
Weekly over 5 weeks
|
Average Social Connection
Time Frame: Weekly over 5 weeks
|
Average social connection as assessed by the relatedness subscale of the Balanced Measure of Psychological Needs.
An average is taken across 6 items, and scores range from 1 to 5 with higher scores indicating greater social connection.
|
Weekly over 5 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Andrew J Fuligni, PhD, University of California, Los Angeles
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
August 24, 2023
Primary Completion (Estimated)
June 1, 2024
Study Completion (Estimated)
July 1, 2024
Study Registration Dates
First Submitted
February 23, 2022
First Submitted That Met QC Criteria
February 23, 2022
First Posted (Actual)
March 4, 2022
Study Record Updates
Last Update Posted (Estimated)
December 6, 2023
Last Update Submitted That Met QC Criteria
November 29, 2023
Last Verified
November 1, 2023
More Information
Terms related to this study
Other Study ID Numbers
- IRB#21-002091
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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