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The Development of Enhancing Coping Resources Program for Reducing Caregiver Burden, Enhancing Coping Strategies, and Reducing Psychological Distress for Caregivers of Advanced Cancer Patients in Bangkok Metropolitan

The Development of Enhancing Coping Resources Program for Reducing Caregiver Burden, Enhancing Coping Strategies, and Reducing Psychological Distress for Caregivers of Advanced Cancer Patients in Bangkok Metropolitan

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
TCTR
Registry ID
TCTR20260429002
Enrollment
72
Registered
2026-04-29
Start date
2026-05-04
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Advanced colorectal cancer Caregiver burden Psychological distress Colorectal neoplasms Caregivers Caregiver burden Stress psychological Coping behavior Digital health Mobile health Chatbot Randomized controlled trial Cortisol

Interventions

Participants will receive the Enhancing Coping Resources Program delivered digitally via a LINE Official Account and chatbot over a 12 week period. During weeks 1 to 2, participants will independently
Experimental Behavioral,No Intervention Other
Enhancing Coping Resources Program,Routine Care

Sponsors

Sarunya Wongkampan
Lead Sponsor
Faculty of Public Health, Mahidol University
Collaborator

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Primary family caregivers of adult patients diagnosed with stage III or IV colorectal cancer with an ECOG performance status of 0 to 2 2. Caregivers aged 18 years or older 3. Residing in Bangkok and surrounding metropolitan areas and living with the patient 4. Able to access and use a smartphone 5. Able to read speak and write Thai 6. Willing to participate and provide informed consent 7. Cognitively able to participate and complete questionnaires with a Mini-Cog score of 3 or higher

Exclusion criteria

Exclusion criteria: 1. Caregivers with cognitive impairment that limits their ability to understand or respond to study assessments 2. Caregivers with functional limitations that prevent participation in study activities 3. Caregivers who are unable to participate in all study procedures

Design outcomes

Primary

MeasureTime frame
Caregiver burden Baseline, immediately post intervention, 6 weeks post intervention Zarit Burden Interview total score

Secondary

MeasureTime frame
Coping strategies Baseline, immediately post intervention, 6 weeks post intervention Brief COPE total score,Psychological distress Baseline, immediately post intervention, 6 weeks post intervention Hospital Anxiety and Depression Scale total score,Cortisol level Baseline, immediately post intervention, 6 weeks post intervention Morning salivary cortisol level

Countries

Thailand

Contacts

Public ContactSarunya Wongkampun

Mahidol University

sarunya.wog@student.mahidol.ac.th023548542

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026