Skip to main content
Clinical Trials/NCT02946697
NCT02946697
Completed
N/A

A Culturally Sensitive Social Support Intervention

M.D. Anderson Cancer Center1 site in 1 country168 target enrollmentJanuary 2015

Overview

Phase
N/A
Intervention
Not specified
Conditions
Breast Cancer
Sponsor
M.D. Anderson Cancer Center
Enrollment
168
Locations
1
Primary Endpoint
Change in Quality of life as assessed by Functional Assessment of Cancer Therapy Scale (FACT)
Status
Completed
Last Updated
last year

Overview

Brief Summary

This study is a randomized controlled trial (RCT) to assess the impact of a culturally based social support program (i.e. Joy Luck Academy, JLA) among Chinese American breast cancer survivors.

Detailed Description

This study is a randomized controlled trial (RCT) to test the health benefits of an education and peer mentor support intervention. Chinese American breast cancer survivors who have completed primary treatment will be randomly assigned to either the intervention group or a control group to receive enhanced usual care while waiting for the JLA. Health outcomes are assessed at baseline, immediately post intervention, and 1 and 4 months follow-ups.

Registry
clinicaltrials.gov
Start Date
January 2015
End Date
October 14, 2024
Last Updated
last year
Study Type
Interventional
Study Design
Crossover
Sex
Female

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Change in Quality of life as assessed by Functional Assessment of Cancer Therapy Scale (FACT)

Time Frame: Baseline before intervention and immediately, 1 month, and 4 months after the intervention

Secondary Outcomes

  • Change in depressive symptoms as assessed by CES-D(Baseline before intervention and immediately, 1 month, and 4 months after the intervention)
  • Change in positive affect as assessed by the PANAS(Baseline before intervention and immediately, 1 month, and 4 months after the intervention)
  • Change in stress as assessed by the Perceived stress scale (PSS)(Baseline before intervention and immediately, 1 month, and 4 months after the intervention)
  • Change in fatigue as assessed by FACIT(Baseline before intervention and immediately, 1 month, and 4 months after the intervention)

Study Sites (1)

Loading locations...

Similar Trials