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The Efficacy of the Caregiver Psychoeducational Consultation Program

Phase 2
Conditions
Depression
Sleep
Interventions
Other: caregiver psychoeducational consultation program (CPCP)
Registration Number
NCT01001884
Lead Sponsor
National Taiwan University Hospital
Brief Summary

Aim:

To examine the effects of the caregiver psychoeducational consultation program in reducing caregiver burdens, depression, sleep quality, and improving the experience in close relationship, positive meaning of illness and quality of life.

This is the 2-year study. The design adopts the randomized controlled trial (RCT). The caregivers of patients with spouse caregivers of resectable metastatic colorectal cancer will be randomly assigned into two groups: one group receiving usual care, another group receiving the caregiver psychoeducational consultation program (CPCP). The usual care includes providing education materials only. Measurement time-points include pre intervention, post intervention, \& then 1, and 3 months after the end of intervention for the maintenance effect.

Detailed Description

To examine the effects of the caregiver psychoeducational consultation program in reducing caregiver burdens, depression, sleep quality, and improving the experience in close relationship, positive meaning of illness and quality of life.

This is the 2-year study. The design adopts the randomized controlled trial (RCT). The caregivers of patients with spouse caregivers of resectable metastatic colorectal cancer will be randomly assigned into two groups: one group receiving usual care, another group receiving the caregiver psychoeducational consultation program (CPCP). The usual care includes providing education materials only. Measurement time-points include pre intervention, post intervention, \& then 1, and 3 months after the end of intervention for the maintenance effect.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
30
Inclusion Criteria
  • Spouse caregivers of patients with resectable colorectal cancer,
  • Those who are willing to participate in the research,
  • Aged above 18.
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Exclusion Criteria
  • Who refuses to participate in this study.
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Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
counselingcaregiver psychoeducational consultation program (CPCP)caregiver psychoeducational consultation program (CPCP)
Primary Outcome Measures
NameTimeMethod
Short-form 12 health-related quality of life questionnairepre intervention, post intervention, 1, and 3,months after the end of the interventions
Secondary Outcome Measures
NameTimeMethod
Caregiver reaction assessmentpre intervention, post intervention, 1, and 3,months after the end of the interventions
Experiences in close relationships scalepre intervention, post intervention, 1, and 3,months after the end of the interventions
Moss sleeping scalepre intervention, post intervention, 1, and 3,months after the end of the interventions
BDI-II depression scalepre intervention, post intervention, 1, and 3,months after the end of the interventions

Trial Locations

Locations (1)

Fei-Hsiu Hsiao

🇨🇳

Taipei, Taiwan

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