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Psychological flexibility intervention for young people with chronic pain and their parents

Application of the psychological flexibility model to young people with chronic pain and their parents

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN18395794
Enrollment
80
Registered
2021-01-15
Start date
2021-01-01
Completion date
Unknown
Last updated
2021-10-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic pain in young people Not Applicable Chronic pain

Interventions

Study 1 uses a cross-sectional survey to unexplored facets of psychological flexibility (PF), design features, and practical methods for enhancing PF for parents and young people with pain conditions.

Sponsors

UCSI University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Malaysian citizen 2. Young people aged 11 to 18 years with pain conditions, and their parents 3. Pain of =3 months duration 4. Able to read and write

Exclusion criteria

Exclusion criteria: 1. Recievingother psychological treatments 2. Acute signs or symptoms 3. Significant levels of depression, anxiety or anger, learning disability, or other difficulties which would affect the ability to participate in the study 4. Significant medical condition that would compromise the ability to participate in the study 5. Unable to attend the full programme 6. Do not provide informed consent

Design outcomes

Primary

MeasureTime frame
1. Parental psychological flexibility measured by the Parent Psychological Flexibility Questionnaire (PPFQ) and Adult Responses to Children’s Symptoms scale (ARCS) at 1 and 14 days 2. Parental psychological stress and well-being measured by the Depression, Anxiety, and Stress inventory (DASS) at 1 and 14 days 3. Children's psychological well-being and functioning measured by the Functional Disability Inventory (FDI), school attendance, and the Child Behavior Checklist) at 1 and 14 days 4. Pain measured by visual analogy scale (VAS) and the Chronic Pain Acceptance Questionnaire adolescent version (CPAQ-A) at 1 and 14 days

Secondary

MeasureTime frame
1. Preferred treatment mode (including face to face or online, group or individuals, continuous or intermittent, short or long duration) measured using a rating scale and qualitative responses with optional open-ended questions at 24 h 2. Parent's belief on the effectiveness of the proposed program, and motivations and barriers to attending the program measured by questionnaire at 24 h 3. Demographic predictors of parents' interest to participate in the program (including the age group of young people with pain conditions, types of pain conditions, the severity of pain conditions, and disability) measured by questionnaire at 24 h

Countries

Malaysia

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026