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
| Type | Name | Description |
|---|---|---|
| BEHAVIORAL | Observation | |
| BEHAVIORAL | Educational 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.