Evaluation of the Building Healthy Life Skills Program

November 3, 2022 updated by: Linda Diane Cameron, University of California, Merced

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

Detailed Description

Community members who are experiencing homelessness and receiving support services from the Merced County Navigation Center and who have enrolled in the center's Building Healthy Life Skills Program will be invited to participate in this intervention evaluation study. The Building Healthy Life Skills program is a 10-week program designed to provide participants with an understanding of how abuse, neglect and household dysfunctions during childhood affect emotional, social, and cognitive well-being; and to provide training in emotion regulation skills, including adaptive emotional processing and expression, mindfulness, and cognitive reappraisal. The sessions are two hours in duration and conducted in classroom style. Open enrollment will be conducted four times a year, serving approximately 60 individuals.

Study Type

Interventional

Enrollment (Anticipated)

60

Phase

  • Phase 2

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

Study Contact Backup

Study Locations

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

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

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

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: 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

This is where you will find people and organizations involved with this study.

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)

October 10, 2022

Primary Completion (Anticipated)

July 1, 2023

Study Completion (Anticipated)

July 1, 2023

Study Registration Dates

First Submitted

October 29, 2022

First Submitted That Met QC Criteria

November 3, 2022

First Posted (Actual)

November 9, 2022

Study Record Updates

Last Update Posted (Actual)

November 9, 2022

Last Update Submitted That Met QC Criteria

November 3, 2022

Last Verified

November 1, 2022

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)?

Undecided

IPD Plan Description

We have not decided on the IPD sharing plan at this point in time.

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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