Mindfulness Program for Adolescents With 22q11DS

Sponsor
Innovation Research & Training (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05849441
Collaborator
(none)
60
2
3

Study Details

Study Description

Brief Summary

The goal of this study is to evaluate the effectiveness of the Aware Program, an online mindfulness education program, with adolescents with 22q11DS and their parents.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Aware Program
N/A

Detailed Description

Parent-adolescent pairs (N=60) will be recruited to participate in a randomized controlled trial. Consent, permission, and/or assent will be sought prior to participation in the study. Participant pairs will be randomized into one of two study arms: intervention and wait-list control. All participants will complete a web-based pre-test questionnaire. Adolescents and parents in the intervention group will then receive access to the Aware Program for four weeks. Approximately 4-5 weeks after completing the pre-test questionnaire, all participants will complete a web-based post-test questionnaire (the post-test for the intervention group will include Consumer Satisfaction questions about the program). Adolescents and parents in the wait-list control group will then have the option of reviewing the Aware Program and will receive access for four weeks. After approximately four weeks, they will have the opportunity to complete the Consumer Satisfaction Questionnaire about the program.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
60 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Health Services Research
Official Title:
Online Mindfulness Intervention for Adolescents With 22q11DS
Anticipated Study Start Date :
Jun 1, 2023
Anticipated Primary Completion Date :
Sep 1, 2023
Anticipated Study Completion Date :
Sep 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Online mindfulness intervention

Participants will have access to the intervention between pre-test and post-test assessments. The intervention, Aware Program, is an online mindfulness education program for adolescents with 22q11DS designed to enhance their coping skills and ability to manage stress and anxiety in healthy ways.

Behavioral: Aware Program
The program includes interactive, multimedia lessons for adolescent participants to learn, practice, and apply different mindfulness skills. Parent-adolescent pairs will have the option to subscribe to a mobile messaging service that includes progress reminders, encouragement, and practice content. Parent participants also have access to online resources to support and monitor their teen's use of the program.

No Intervention: Wait-List Control

Participants will not have access to the online mindfulness intervention between the pre-test and post-test assessments. After completing the post-test questionnaires, participants in the wait-list control group will receive access to the online mindfulness intervention (Aware Program).

Outcome Measures

Primary Outcome Measures

  1. Change from baseline in adolescents' coping skills [Baseline and Week 4]

    Adolescents will be asked to respond to 34 questions (e.g., Try to think of different ways to solve it; 1 = Never; 5 = Always) that assess their coping in response to stressors across 5 domains: Seeking Social Support, Problem Solving, Distancing, Externalizing, and Internalizing. Three items related to mindfulness skills will be included as a mindfulness subscale. Responses will be averaged across each domain and the minimum scale score is 1 and the maximum scale score is 5. Higher scores indicate greater use of the coping strategy.

  2. Change from baseline in adolescents' emotion regulation [Baseline and Week 4]

    Adolescents will be asked to respond to 10 questions (e.g., I keep my emotions to myself; 1 = Strongly disagree; 7 = Strongly agree) that assess their use of two emotion regulation strategies: Cognitive Reappraisal and Suppression. Responses will be averaged across each strategy and the minimum scale is 1 and the maximum scale score is 7. Higher scores indicate greater use of the emotion regulation strategy.

  3. Change from baseline in adolescents' emotional self-efficacy [Baseline and Week 4]

    Adolescents will be asked to respond to 27 questions (e.g., I can tell when my feelings change; 1 = Not confident at all; 5 = Very confident) that assess their beliefs about their ability to understand and manage emotions. The measure has four factors: Using and managing your own emotions; Identifying and understanding your own emotions; Dealing with emotions in others; Perceiving emotion through facial expressions and body language. Responses will be averaged across the four factors and the minimum scale score is 1 and the maximum scale score is 5. Higher scores indicate greater emotional self-efficacy.

  4. Change from baseline in adolescents' general anxiety [Baseline and Week 4]

    Adolescents will be asked to respond to 7 items that assess general anxiety (e.g., Over the last two weeks, how often have you been bothered by the following problems… feeling nervous, anxious, or on edge; 0 = Not at all, 1 = Several days, 2 = More than half the days, 3 = Nearly every day). Responses will be averaged and the minimum scale score is 0 and the maximum scale score is 3. Higher scores indicate greater general anxiety.

  5. Change from baseline in adolescents' social anxiety [Baseline and Week 4]

    Adolescents will be asked to respond to 18 items (e.g., It's hard for me to ask others to do things with me; 1 = Not at all; 5 = All the time) that assess social anxiety. The measure has three factors: Fear of Negative Evaluation, Social Avoidance and Distress-New; Social Avoidance and Distress. Responses will be averaged across the three factors and the minimum scale score is 1 and the maximum scale score is 5. Higher scores indicate greater social anxiety.

  6. Change from baseline in adolescents' wellbeing [Baseline and Week 4]

    Adolescents will be asked to respond to a total of 7 items that assess their overall health and wellbeing. Adolescents will respond to 4 items (e.g., In general, would you say your quality of life is…; 5 = Excellent, 1 = Poor); 1 item (e.g., How often do you feel really sad; 5 = Never; 1 = Always); and 2 items (e.g., How often do you have fun with friends?; 5 = Always; 1 = Never). Responses will be averaged and the minimum scale score is 1 and the maximum scale score is 5. Higher scores indicate greater wellbeing.

  7. Change from baseline in parent report of adolescents' emotion regulation [Baseline and Week 4]

    Parents will be asked to respond to 24 questions (e.g., Responds positively to neutral or friendly overtures by peers; 1= Never; 4 = Always) that assess parent ratings of their adolescents' emotion regulatory abilities. There are two subscales for this measure: Emotion Regulation and Negativity. Responses will be averaged across the two subscales and the minimum scale score is 1 and the maximum scale score is 4. Higher scores indicate greater use of the emotion regulation strategy.

  8. Change from baseline in parent report of adolescents' executive functioning [Baseline and Week 4]

    Parents will be asked to respond to 24 questions (e.g., Has difficulty thinking ahead or learning from experience; 1 = Definitely not true; 5 = Definitely true) that assess parent ratings of their adolescents' executive functioning. There are four subscales: Working Memory, Planning, Inhibition, and Regulation. Responses will be averaged across the four subscales and the minimum scale score is 1 and the maximum scale score is 5. Higher scores indicate greater executive functioning.

  9. Change from baseline in parent report of adolescents' anxiety [Baseline and Week 4]

    Parents will be asked to respond to 8 questions (e.g., My child worries about things; 1 = Never; 4 = Always) that assess parent ratings of their adolescents' anxiety. Responses will be averaged and the minimum scale score is 1 and the maximum scale score is 4. Higher scores indicate greater anxiety.

  10. Change from baseline in parent report of adolescents' wellbeing [Baseline and Week 4]

    Parents will be asked to respond to a total of 7 items that assess parent ratings of their adolescents' overall health and wellbeing. Parents will respond to 4 items (e.g., In general, would you say your child's quality of life is…; 5 = Excellent, 1 = Poor); 1 item (e.g., How often does your child feel really sad; 5 = Never; 1 = Always); and 2 items (e.g., How often does your child have fun with friends?; 5 = Always; 1 = Never). Responses will be averaged and the minimum scale score is 1 and the maximum scale score is 5. Higher scores indicate greater wellbeing.

Eligibility Criteria

Criteria

Ages Eligible for Study:
12 Years to 19 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
To be included in the study, youth must:
  • Have received a diagnosis of 22Q11.DS (also known as VeloCardioFacial Syndrome or DiGeorge syndrome)

  • Be between the ages of 12 and 19 years old

  • Have an IQ of greater than or equal to 60

  • Have regular internet and computer access

  • Speak and read English (all study and program materials are in English)

To be included in the study, parents must:
  • Have a participating youth in the study

  • Read fluently in English (all study and program materials are in English)

Exclusion Criteria:
  • Only one parent per youth may participate

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Innovation Research & Training

Investigators

  • Principal Investigator: Alison Parker, PhD, Innovation Research & Training

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Innovation Research & Training
ClinicalTrials.gov Identifier:
NCT05849441
Other Study ID Numbers:
  • MindfulnessinTeens-SBIR-23-001
First Posted:
May 8, 2023
Last Update Posted:
May 8, 2023
Last Verified:
Apr 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 8, 2023