Skip to main content
Clinical Trials/NCT01595243
NCT01595243
Completed
Not Applicable

Effects of Telephone Follow- up Consultations on Discharged Liver Cancer Following Non-surgical Treatment

National Taiwan University Hospital1 site in 1 country254 target enrollmentOctober 2009

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Hepatocellular Carcinoma
Sponsor
National Taiwan University Hospital
Enrollment
254
Locations
1
Primary Endpoint
12-Item Short Form Survey
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

The aims of this three-year study are to:

  1. From patients and family perspective to explore the needs for home care after receiving TACE, PEI, and RFA
  2. Develop a telephone follow-up and consultation program and examine its effect on self-efficacy, anxiety, depression and quality of life in liver cancer patients receiving non-surgical treatment.

Detailed Description

In the first year, a longitudinal mixed method with quantitative and qualitative method will be used. The Distress Management Tool, the Hospital Anxiety and Depression Scale, and the Short Form-12 quality of life will be used to assess patients' care needs, anxiety, depression, and quality of life in the quantitative method. Data will be analyzed by descriptive, Pearson's Correlation, and Stepwise Regression for each time point. Tape-recorded and in-depth interviews with semi-structured interview guidelines will be used in qualitative method to interview the cancer patients who are scheduled to be discharged after treatment. Content analysis will be used to analyze the interview content. In the second and third year, randomized control trial will be used to recruit eligible subjects from inpatients in oncology wards in one medical center in Taipei. The eligible subjects will be randomized into a control or experimental group. The patients in the control group will receive usual care and those in the experimental group will receive seven instances of telephone follow-up or face-to-face education (the day before discharge and during the first, second, third, fourth, sixth, and eighth weeks after discharge).Data will be analyzed by independent t-test, one-way analysis of variance, and generalized estimating equations.

Registry
clinicaltrials.gov
Start Date
October 2009
End Date
August 2014
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients with liver cancer in non-surgical treatment
  • Aged above 18
  • Those who are wiling to participate in the research

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

12-Item Short Form Survey

Time Frame: 3 months after discharge

Quality of life

Study Sites (1)

Loading locations...

Similar Trials