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Clinical Trials/NCT01519895
NCT01519895
Completed
Phase 2

Effectiveness of Telephone-based Intervention on Distress, Burden and Quality of Life of Chinese Caregivers of Colorectal Cancer Patients

Hospital Authority, Hong Kong1 site in 1 country140 target enrollmentJune 2011

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Psychological Stress
Sponsor
Hospital Authority, Hong Kong
Enrollment
140
Locations
1
Primary Endpoint
Distress level
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

The purpose of this study is to assess the effectiveness of the telephone intervention program for caregivers of colorectal cancer.

Detailed Description

telephone Intervention refer to provide counseling and education to caregivers of colorectal cancer by mode of telephone

Registry
clinicaltrials.gov
Start Date
June 2011
End Date
December 2012
Last Updated
11 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Hospital Authority, Hong Kong
Responsible Party
Principal Investigator
Principal Investigator

Shum Nga Fan

Department of Surgery, Colorectal Specialist Nurse, Principal Investigator

Hospital Authority, Hong Kong

Eligibility Criteria

Inclusion Criteria

  • Family members with newly diagnosed colorectal cancer within the past 4 week and treated in Queen Mary Hospital
  • Self identified as formal or informal family caregivers
  • Over 18 years old
  • Cantonese speaking

Exclusion Criteria

  • Cognitive disability
  • Domestic helpers or maids
  • Non Chinese

Outcomes

Primary Outcomes

Distress level

Time Frame: Change of distress level at pre-discharged(base-line) and 2 weeks and 4 weeks and 8 weeks post intervention

Effect of telephone intervention on distress level measured at pre-discharged(baseline) and 2 weeks and 4 weeks and 8 weeks post intervention .

Secondary Outcomes

  • Burden of care(Measured at pre-discharged(base-line) and 2 weeks and 4 weeks and 8 weeks post intervention)
  • Quality of life(Measured at pre-discharged(base-line) and 2 weeks and 4 weeks and 8 weeks post intervention)

Study Sites (1)

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