- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02770898
Improving Family Holistic Health in Probationers
Improving Family Holistic Health in Probationers- a Mixed Methods Evaluation
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
To enhance individual and family well-being among probationers, family life and health education, including the skills and knowledge for physical exercise, healthy family functioning, strong communication skills, healthy interpersonal relationships, and positive self-esteem, should be strengthened and promoted. Based on the strong foundation of the FAMILY projects conducted by our research team in the past years, this project seeks to promote "FAMILY holistic health" for targeted families (i.e. probationers). The holistic health interventions are interactive and designed for behavioral changes to enhance individual well-being and encourage positive and sustainable health actions among family members. Thus, it is expected ultimately that the participants and their family members could enhance their family happiness, health, and harmony (3Hs). In sum, the project has the following contributions:
- Strengthen evidence-based practice Hong Kong probation-related topics are scarcely studied. There is a need for rigorous studies to build and strengthen evidence-base for probation services. This study will be one of the first studies to evaluate the effectiveness of probation services on individual well-being and family well-being utilizing a mixed-methods approach.
- Stakeholder engagement Stakeholders will be engaged throughout the research process. This promotes co-learning and empowering process, builds on strengths and resources within the community, and integrates knowledge and intervention for the mutual benefit of all partners.
- Train-the-trainer program Training will be provided to probation officers and/or workers at the Social Welfare Department. The result of this train-the-trainers program is that front-line service workers will increase and enhance their knowledge and skills to independently and effectively carry out interventions. Probation officers will act as role models for probationers and continue to implement our knowledge and techniques in their future interventions.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Hong Kong, China
- The University of Hong Kong
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Be an existing probationer with 6 months of term remaining
- Reading and writing abilities for questionnaire completion
- Have family members that are based in Hong Kong (the rationale is that one of the secondary outcome is to improve family relations)
- Probationer does not have a developmental or intellectual disability
- Probationer aged 13 and above (the rationale is that youth under 12 years of age may not have the cognitive ability to complete questionnaires)
Exclusion Criteria:
- Sexual offenders
- Drug offenders
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: Brief Intervention
The brief intervention is individual focus and consists of three main components, which include enhancing the individual personal attributes such as participant's knowledge, values, and behaviors related to physical exercise.
Second, the intervention will promote changes in behavioral attributes by providing opportunities and experience in goal setting, skills development in physical exercise and self-monitoring.
Finally, the brief intervention promotes family relations and well-being by encouraging individuals to share their knowledge and increase physical activities with other family members.
The brief intervention will be delivered by the probation officer during regular monthly consultation.
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Interventions for probationers will aim to promote physical and psychosocial health, family relationships and Family 3H (happiness, harmony and health).
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Experimental: Combined Intervention
Participants allocated to the combined intervention will receive the individual brief intervention and participate in a community group program.
The components in the brief intervention will also be reinforced in the group program.
The group nature is designed to create an environment that is supportive of physical exercise, through role models, peer support, and encourages families to exercise with probationers.
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Interventions for probationers will aim to promote physical and psychosocial health, family relationships and Family 3H (happiness, harmony and health).
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No Intervention: Care-as-usual
Participants allocated to Care-as-usual arm will receive their usual services.
Participants will be offered the combined interventions upon completion of 3-months follow up assessment.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Changes in Individual well-being (self-esteem, self-efficacy)
Time Frame: T1 (baseline), T2 (one month follow-up), T3 (three months follow-up)
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Individual well-being will be assessed by the Rosenberg Self-esteem Scale.
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T1 (baseline), T2 (one month follow-up), T3 (three months follow-up)
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Physical health
Time Frame: T1 (baseline), T2 (one month follow-up), T3 (three months follow-up)
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Physical health will be assessed by the SF-12v2 health survey.
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T1 (baseline), T2 (one month follow-up), T3 (three months follow-up)
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Psychosocial health
Time Frame: T1 (baseline), T2 (one month follow-up), T3 (three months follow-up)
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Psychosocial health will be assessed by the SF-12v2 health survey.
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T1 (baseline), T2 (one month follow-up), T3 (three months follow-up)
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Behaviours on physical exercise (Adapted version of IPAC)
Time Frame: T1 (baseline), T2 (one month follow-up), T3 (three months follow-up)
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Theme-related behaviours will be assessed by behavioural indicators.
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T1 (baseline), T2 (one month follow-up), T3 (three months follow-up)
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Family health, happiness and harmony (3Hs)
Time Frame: T1 (baseline), T2 (one month follow-up), T3 (three months follow-up)
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Family 3Hs will be assessed by the family well-being scale.
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T1 (baseline), T2 (one month follow-up), T3 (three months follow-up)
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Family relations
Time Frame: T1 (baseline), T2 (one month follow-up), T3 (three months follow-up)
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Family relations will be assessed by the family APGAR scale.
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T1 (baseline), T2 (one month follow-up), T3 (three months follow-up)
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Satisfaction towards the program (Self-generated satisfaction scale)
Time Frame: T1 (baseline), T2 (one month follow-up), T3 (three months follow-up)
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Satisfaction towards the program will be assessed by a program evaluation measure.
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T1 (baseline), T2 (one month follow-up), T3 (three months follow-up)
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Collaborators and Investigators
Sponsor
Publications and helpful links
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
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
- UW 15-249
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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