Clinical Trials Directory

Trials / Terminated

TerminatedNCT00002668

Pain Control in Patients With Recurrent or Metastatic Breast or Prostate Cancer

PATIENT SKILLS FOR CANCER PAIN CONTROL IN PATIENTS WITH METASTATIC BREAST OR PROSTATE CANCER

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
13 (actual)
Sponsor
Eastern Cooperative Oncology Group · Network
Sex
All
Age
18 Years – 120 Years
Healthy volunteers
Not accepted

Summary

RATIONALE: An outpatient educational and behavioral skills training program may help patients with metastatic breast or prostate cancer live longer and more comfortably. PURPOSE: This randomized clinical trial studies whether an outpatient educational and behavioral skills training program will improve pain control in patients who have metastatic or recurrent breast or prostate cancer.

Detailed description

OBJECTIVES: * Evaluate the feasibility of implementing an outpatient education and behavioral skills training program for pain control in a multi-institution setting. * Evaluate whether patient education and behavioral skills training improve cancer pain control in patients with recurrent or metastatic breast or prostate cancer. * Amend the protocol, with the approval of the Division of Cancer Prevention and Control, to a groupwide 3-arm study if analysis demonstrates feasibility and potential efficacy of the patient education and behavioral skills training program. OUTLINE: This is a randomized study. Patients are stratified according to diagnosis (breast vs prostate cancer), initial "pain worst" score (4-6 vs 7 or higher), and participating institution. Patients are randomized to 1 of 2 treatment arms. * Arm I: Patients receive standard pain management. * Arm II: Patients receive educational intervention (booklets, audiotapes, and videotapes) and behavioral skills training (including a schedule of practice relaxation sessions) in addition to standard pain management. Patients receive a follow-up phone call within 48-72 hours of intervention to review pain status. Patients on both arms undergo pain and psychological assessments on days 1 and 15. PROJECTED ACCRUAL: A total of 96 patients (48 per arm) will be accrued for this study.

Conditions

Interventions

TypeNameDescription
BEHAVIORALObservation
BEHAVIORALEducational Intervention and Behavioral Skills Training

Timeline

Start date
1996-02-14
Primary completion
1998-09-01
Completion
1998-09-01
First posted
2003-01-27
Last updated
2023-06-22

Locations

18 sites across 4 countries: United States, Australia, Peru, Puerto Rico

Source: ClinicalTrials.gov record NCT00002668. Inclusion in this directory is not an endorsement.