Improving Family Holistic Health in Probationers

May 3, 2018 updated by: The University of Hong Kong

Improving Family Holistic Health in Probationers- a Mixed Methods Evaluation

Evaluating the impact of probation on probationers is necessary for both effective practice of probation officers and their assessment of the success of their work. At present, there are limited studies that have evaluated the impact of probation services on probationers and their family. There are even fewer studies that have examined interventions on probationers' well-being and family relations in a Chinese society. Compared with the general population, probationers are associated with poorer mental (e.g., depression, lower levels of self-esteem, high level of stress) and physical health, and often experience higher levels of family conflict, and poorer quality of family relationships. Given the vulnerabilities, there is a need to strengthen and promote healthy lifestyle and enhance individual and family well-being among probationers. As part of the FAMILY project, the current study focuses on "FAMILY Holistic Health" which emphasizes a comprehensive approach to improving physical, mental, and social health and well-being. This project will be conducted as a pilot project in the Social Welfare Department (SWD) in the Eastern District of Hong Kong. Interventions will be delivered to promote and enhance probationer's wellbeing, as well as enhancing FAMILY 3Hs (Happiness, Health, and Harmony). Training programs will be provided to probation officers and/or workers of SWD in order to equip them with knowledge and skills in implementing health-related family intervention programs.

Study Overview

Status

Completed

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:

  1. 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.
  2. 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.
  3. 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

Interventional

Enrollment (Actual)

463

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Hong Kong, China
        • The University of Hong Kong

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

13 years and older (Child, Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

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

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: Health Services Research
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
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.
Interventions for probationers will aim to promote physical and psychosocial health, family relationships and Family 3H (happiness, harmony and health).
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.
Interventions for probationers will aim to promote physical and psychosocial health, family relationships and Family 3H (happiness, harmony and health).
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.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Changes in Individual well-being (self-esteem, self-efficacy)
Time Frame: T1 (baseline), T2 (one month follow-up), T3 (three months follow-up)
Individual well-being will be assessed by the Rosenberg Self-esteem Scale.
T1 (baseline), T2 (one month follow-up), T3 (three months follow-up)

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)
Physical health will be assessed by the SF-12v2 health survey.
T1 (baseline), T2 (one month follow-up), T3 (three months follow-up)
Psychosocial health
Time Frame: T1 (baseline), T2 (one month follow-up), T3 (three months follow-up)
Psychosocial health will be assessed by the SF-12v2 health survey.
T1 (baseline), T2 (one month follow-up), T3 (three months follow-up)
Behaviours on physical exercise (Adapted version of IPAC)
Time Frame: T1 (baseline), T2 (one month follow-up), T3 (three months follow-up)
Theme-related behaviours will be assessed by behavioural indicators.
T1 (baseline), T2 (one month follow-up), T3 (three months follow-up)
Family health, happiness and harmony (3Hs)
Time Frame: T1 (baseline), T2 (one month follow-up), T3 (three months follow-up)
Family 3Hs will be assessed by the family well-being scale.
T1 (baseline), T2 (one month follow-up), T3 (three months follow-up)
Family relations
Time Frame: T1 (baseline), T2 (one month follow-up), T3 (three months follow-up)
Family relations will be assessed by the family APGAR scale.
T1 (baseline), T2 (one month follow-up), T3 (three months follow-up)
Satisfaction towards the program (Self-generated satisfaction scale)
Time Frame: T1 (baseline), T2 (one month follow-up), T3 (three months follow-up)
Satisfaction towards the program will be assessed by a program evaluation measure.
T1 (baseline), T2 (one month follow-up), T3 (three months follow-up)

Collaborators and Investigators

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

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the 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

July 1, 2015

Primary Completion (Actual)

March 1, 2017

Study Completion (Actual)

July 1, 2017

Study Registration Dates

First Submitted

November 23, 2015

First Submitted That Met QC Criteria

May 10, 2016

First Posted (Estimate)

May 12, 2016

Study Record Updates

Last Update Posted (Actual)

May 4, 2018

Last Update Submitted That Met QC Criteria

May 3, 2018

Last Verified

May 1, 2018

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)?

UNDECIDED

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.

Clinical Trials on Self-esteem

Clinical Trials on Family Holistic Health

Subscribe