- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07591636
ACT Dad Interview: ACT for Fathers of Children With Special Needs
A Qualitative Study to Develop a Protocol Using Acceptance and Commitment Therapy (ACT) for Fathers of Children With Special Needs in Improving Their Psychological Flexibility and Mental Health
The goal of this qualitative study is to develop a therapy protocol for fathers of children with special needs in Hong Kong. The therapy is called Acceptance and Commitment Therapy (ACT), which helps people cope with difficult emotions by building psychological flexibility - the ability to accept and adjust to hard situations. The main questions it aims to answer are:
- What are the experiences and needs of fathers raising children with special needs?
- What content and format of an ACT programme would be most helpful for these fathers?
Researchers will conduct focus group interviews with two groups of participants: fathers raising children with special needs and social workers who work with these families. The interviews will take about 60 to 90 minutes each.
Participants will:
- Take part in a recorded focus group interview
- Share their experiences, challenges, and views on what an ACT program should include
The findings will be used to develop a protocol for an ACT programme to improve the mental health of fathers raising children with special needs.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Ka Wai Katherine LAM, Doctor of Philosophy
- Phone Number: +852 27666420
- Email: kw-katherine.lam@polyu.edu.hk
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Informants will include 2 groups, 1) fathers rearing children with special needs and 2) social workers.
For fathers,
Inclusion Criteria:
- are the biological fathers of children aged 2 to 12 years,
- are with a child having a formal diagnosis of a developmental disability, including autism spectrum disorder, attention deficit/hyperactivity disorder, intellectual disability, or related neurodevelopmental conditions,
- are able to speak Cantonese and read Chinese.
Exclusion Criteria:
- Fathers with physical or cognitive impairment
- Father with learning problems as identified from NGO or related medical records
For social workers,
Inclusion Criteria:
- have experience in working with biological fathers of children aged 2 to 12 years who have a formal diagnosis of a developmental disability, including autism spectrum disorder, attention deficit/hyperactivity disorder, intellectual disability, or related neurodevelopmental conditions,
- are able to speak Cantonese and read Chinese.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
SEN father and social workers
|
Participants will take part in a 60 to 90-minute, video-recorded, semi-structured focus group interview conducted in Cantonese.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Psychological flexibility
Time Frame: immediately after the interview
|
Qualitative method, conducted in the form of individual semi-structured interviews.
|
immediately after the interview
|
|
Mental Health
Time Frame: immediately after the interview
|
Qualitative method, conducted in the form of individual semi-structured interviews.
|
immediately after the interview
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
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
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- ACT Dad interview
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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