Adolescent Acts of Kindness Intervention

Sponsor
University of California, Los Angeles (Other)
Overall Status
Completed
CT.gov ID
NCT03322397
Collaborator
(none)
97
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15.2
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Study Details

Study Description

Brief Summary

Adolescents will complete a 4-week intervention, during which they will either complete a kind act for others, complete a kind act for themselves, or report their daily activities three days per week. Psychological and physiological measures will be indexed before and after the intervention.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Self-Focused Acts of Kindness Intervention
  • Behavioral: Other-Focused Acts of Kindness Intervention
  • Behavioral: Daily Reports
N/A

Detailed Description

Stress and early adversity have been found to influence immune function via enhanced expression of the conserved transcriptional response to adversity (CTRA) genetic profile. Expression of this genetic profile was reduced in adults who completed a prosocial behavior intervention. This project aims to implement this intervention in adolescents. 90 high school students will be recruited and assigned to one of three groups (30/group). Participants will either conduct 3 acts of kindness for themselves, conduct 3 acts of kindness for others, or report about their day 3 times 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 come into the lab twice, once before and once after the 4-week intervention. During these lab sessions participants will complete survey measures, have their heart rate measured, and have a blood draw conducted by a trained phlebotomist. Participants' parents will also complete a brief survey 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 health and the psychological mechanisms underlying these effects. At the second study visit, participants will be given the opportunity to donate part of their study payment to a charity to measure prosociality. Any donations will be vetted with the psychology department's accounting group prior to making any donations in the university's name. Scott Monatlik, Director, Tax and Information Practices, at smonatlik@finance.ucla.edu or (310) 794-6724 will be contacted and information regarding the appropriate steps to take to ensure that the donation is made to an acceptable charity prior to any donations. Actual helping behavior (donations) is measured to provide an ecologically valid experimental evaluation of prosociality rather than traditional metrics of computerized, fictional giving. Conceptual frameworks from developmental and health psychology guide the hypothesis that prosocial behavior will influence adolescents.

Study Design

Study Type:
Interventional
Actual Enrollment :
97 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
90 participants will randomly be assigned to one of three interventions. Participants will complete a 4-week intervention. All outcomes will be measured before and after the intervention, and some psychological measures will be collected weekly throughout the intervention.90 participants will randomly be assigned to one of three interventions. Participants will complete a 4-week intervention. All outcomes will be measured before and after the intervention, and some psychological measures will be collected weekly throughout the intervention.
Masking:
Single (Participant)
Masking Description:
Participants will be told that the investigatos are studying the daily lives of teens. They will not be informed of the other arms of the experiment.
Primary Purpose:
Basic Science
Official Title:
Study of Daily Life and Health
Actual Study Start Date :
Oct 8, 2017
Actual Primary Completion Date :
Jan 13, 2019
Actual Study Completion Date :
Jan 13, 2019

Arms and Interventions

Arm Intervention/Treatment
Experimental: Kindness to Others

Participants will complete the 'Other-Focused Acts of Kindness Intervention' by performing acts of kindness for others. They 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.

Behavioral: Other-Focused Acts of Kindness Intervention
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.

Active Comparator: Kindness to Self

Participants will complete the 'Self-Focused Acts of Kindness Intervention' by performing acts of kindness for themselves. They 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.

Behavioral: Self-Focused Acts of Kindness Intervention
Participants engage in positive behaviors by completing acts of kindness for themselves 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.

Behavioral: Daily Reports
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.

Outcome Measures

Primary Outcome Measures

  1. Average Positive Affect [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.

Secondary Outcome Measures

  1. Inflammatory Gene Expression [Baseline and one-week post intervention (elapsed time of 5 weeks)]

    Change in inflammatory gene expression from baseline to one week following the intervention as assessed by assays of the conserved transcriptional response to adversity profile of gene expression in leukocytes.

  2. Average Psychological Flourishing [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.

  3. Average Negative Affect [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.

Other Outcome Measures

  1. Average Stress [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.

  2. Sleep Quality [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.

  3. Inflammatory Composite [Baseline and one-week post intervention (elapsed time of 5 weeks)]

    Change in inflammation from baseline to one week following the intervention as assessed by the concentration of a variety of inflammatory cytokines (e.g., IL-6, IL-1).

  4. Respiratory Sinus Arrythmia (RSA) [Baseline and one-week post intervention (elapsed time of 5 weeks)]

    Change in RSA from baseline to one week following the intervention as assessed by high-frequency heart rate variability during paced breathing.

  5. Average Social connection [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.

  6. Donation [5 weeks]

    Donation as assessed by the amount of money participants donated (maximum of $10) to a charity for foster youth.

Eligibility Criteria

Criteria

Ages Eligible for Study:
14 Years to 17 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Between the ages of 14-17
Exclusion Criteria:
  • None

Contacts and Locations

Locations

Site City State Country Postal Code
1 Adolescent Development Lab at UCLA Los Angeles California United States 90066

Sponsors and Collaborators

  • University of California, Los Angeles

Investigators

  • Principal Investigator: Andrew Fuligni, PhD, Professor

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Andrew J. Fuligni, PhD, Principal Investigator, University of California, Los Angeles
ClinicalTrials.gov Identifier:
NCT03322397
Other Study ID Numbers:
  • 17-001018
First Posted:
Oct 26, 2017
Last Update Posted:
Feb 21, 2019
Last Verified:
Feb 1, 2019
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Andrew J. Fuligni, PhD, Principal Investigator, University of California, Los Angeles
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 21, 2019