- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05611060
Evaluation of the Building Healthy Life Skills Program
Building Healthy Life Skills for Merced County Navigation Center
The goal of this intervention trial is to learn test whether participation in the Building Health Life Skills Program leads to improvements in psychological well-being and stress management skills for people who are experiencing homelessness and housing insecurity. The main questions it aims to answer are:
- Will participation in the Building Healthy Life Skills Program lead to better skills in managing negative emotions?
- Will participation in the Building Healthy Life Skills Program lead to improvements in psychological well-being, sleep quality, and health-related quality of life?
Participants will be asked to complete three surveys: one prior to the first session of the program, one at the end of the program, and one three months later. The surveys include measures of skills for managing negative emotions, mood states, sleep quality, health-related quality of life, illness experiences, and history of childhood adversity.
Study Overview
Status
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Anticipated)
Phase
- Phase 2
Contacts and Locations
Study Contact
- Name: Linda D Cameron, Ph.D.
- Phone Number: 209-626-6892
- Email: lcameron@ucmerced.edu
Study Contact Backup
- Name: Marisela Yepez, B.S.
- Phone Number: 209-228-2252
- Email: myepez5@ucmerced.edu
Study Locations
-
-
California
-
Merced, California, United States, 95343
- Recruiting
- University of California Merced
-
Contact:
- Linda D Cameron, Ph.D.
- Phone Number: 209-626-6892
- Email: lcameron@ucmerced.edu
-
Contact:
- Marisela Yepez, B.A.
- Email: myepez5@ucmerced.edu
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Individuals who are receiving support services from the Merced County Navigation Center due their current experiences of housing insecurity or homelessness, and
- have enrolled in the Building Healthy Life Skills program
Exclusion Criteria:
- Individuals under the age of 18 years and those who cannot speak English or Spanish
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in health-related quality of life as assessed by the SF-12, for which scores range from 0 to 100 with higher scores reflecting better quality of life
Time Frame: Assessed at baseline, immediately following completion of the intervention, and 3 months following intervention completion
|
Health-related quality of life as assessed by the SF 12
|
Assessed at baseline, immediately following completion of the intervention, and 3 months following intervention completion
|
|
Change in depressive symptoms as assessed by the Center for Epidemiological Studies Depression measure, for which averaged rating scores range from 0 to 3 with higher scores reflecting more depressive symptoms
Time Frame: Assessed at baseline, immediately following completion of the intervention, and 3 months following intervention completion
|
Scores on the Center for Epidemiological Studies Depression measure
|
Assessed at baseline, immediately following completion of the intervention, and 3 months following intervention completion
|
|
Change in stress as assessed by the Perceived Stress Scale, for which averaged rating scores range from 1 to 5 with higher scores reflecting greater stress
Time Frame: Assessed at baseline, immediately following completion of the intervention, and 3 months following intervention completion
|
Scores on the Perceived Stress Scale
|
Assessed at baseline, immediately following completion of the intervention, and 3 months following intervention completion
|
|
Change in rumination as an emotion regulation behavior as assessed by the Rumination and Reflections Questionnaire,for which averaged rating scores range from 1 to t with higher scores reflecting more rumination
Time Frame: Assessed at baseline, immediately following completion of the intervention, and 3 months following intervention completion
|
Scores on the Rumination and Reflections Questionnaire
|
Assessed at baseline, immediately following completion of the intervention, and 3 months following intervention completion
|
|
Change in emotional suppression as assessed by the Cortauld Emotional Control Scale (scores range is 1-4, higher scores reflect higher suppression) and the Emotion Regulation Questionnaire (scores range is 1-5, higher scores reflect higher suppression)
Time Frame: Assessed at baseline, immediately following completion of the intervention, and 3 months following intervention completion
|
Scores on the Cortauld Emotional Control Scale and the Emotion Regulation Questionnaire
|
Assessed at baseline, immediately following completion of the intervention, and 3 months following intervention completion
|
|
Change in mindfulness as an emotional regulation tendency as assessed by the Mindful Awareness Attention Scale, for which averaged rating scores range from 1 to 5 with higher scores reflecting greater mindfulness tendencies
Time Frame: Assessed at baseline, immediately following completion of the intervention, and 3 months following intervention completion
|
Scores on the Mindful Awareness Attention Scale
|
Assessed at baseline, immediately following completion of the intervention, and 3 months following intervention completion
|
|
Change in cognitive reappraisal as an emotion regulation strategy as assessed by the Emotion Regulation Questionnaire, for which averaged rating scores range from 1 to 5 with higher scores reflecting higher use of cognitive reappraisal
Time Frame: Assessed at baseline, immediately following completion of the intervention, and 3 months following intervention completion
|
Scores on the Emotion Regulation Questionnaire
|
Assessed at baseline, immediately following completion of the intervention, and 3 months following intervention completion
|
|
Change in general self-efficacy as assessed by the General Self-Efficacy Survey, for which averaged rating scores range from 1 to 5 with higher scores reflecting higher sense of self-efficacy in managing challenging situations
Time Frame: Assessed at baseline, immediately following completion of the intervention, and 3 months following intervention completion
|
Scores on the General Self-Efficacy Survey
|
Assessed at baseline, immediately following completion of the intervention, and 3 months following intervention completion
|
|
Change in resilience as assessed by the Ego Resilience 89, for which averaged rating scores range from 1 to 5 with higher scores reflecting higher resilience in managing challenging situations
Time Frame: Assessed at baseline, immediately following completion of the intervention, and 3 months following intervention completion
|
Scores on the Ego Resilience 89
|
Assessed at baseline, immediately following completion of the intervention, and 3 months following intervention completion
|
|
Change in sleep quality as assessed by the Pittsburgh Sleep Quality Inventory, for which averaged rating scores range from 0 to 21 with higher scores reflecting poorer sleep quality
Time Frame: Assessed at baseline, immediately following completion of the intervention, and 3 months following intervention completion
|
Scores on the Pittsburgh Sleep Quality Inventory
|
Assessed at baseline, immediately following completion of the intervention, and 3 months following intervention completion
|
|
Change in physical health as assessed by self-reported number of sick days in the past month (ranging from 0 to 31) and a the frequency of 17 symptoms each rated 1 to 5 and higher averaged rating scores reflecting higher symptom loads
Time Frame: Assessed at baseline, immediately following completion of the intervention, and 3 months following intervention completion
|
Scores on a symptom checklist and number of sick days
|
Assessed at baseline, immediately following completion of the intervention, and 3 months following intervention completion
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- Cameron2022
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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