Clinical Trials Directory

Trials / Completed

CompletedNCT00057733

Stress Management Training in Patients Undergoing Radiation Therapy for Cancer

Stress Management Training For Patients Undergoing Radiotherapy

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
Sponsor
University of South Florida · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

RATIONALE: Stress management techniques such as muscle relaxation, guided imagery, and abdominal breathing may improve quality of life and decrease emotional distress in patients who are undergoing radiation therapy for cancer. PURPOSE: Randomized clinical trial to determine the effectiveness of stress management training in helping cancer patients cope with the emotional distress of radiation therapy.

Detailed description

OBJECTIVES: Primary * Determine whether a modified version of a self-administered stress management training intervention, previously found to be of benefit in chemotherapy patients, is effective in improving quality of life and decreasing psychological distress (anxiety and depression) in patients with cancer who are undergoing radiotherapy. Secondary * Compare the efficacy of this intervention on improving quality of life and decreasing psychological distress (anxiety and depression) in male vs female patients. OUTLINE: This is a randomized, multicenter study. Patients are randomized to 1 of 2 treatment arms. * Arm I: Patients receive self-administered stress management training (SSMT) in 3 stress management techniques (progressive muscle relaxation training and guided imagery, abdominal breathing, and coping skills) adapted specifically for use during radiotherapy. Patients initially receive a 5-minute standardized presentation regarding the nature and purpose of SSMT. Patients then receive information and instruction regarding the three stress management techniques comprising a videotape, audiotape, and brochure. Patients also receive their institution's usual psychosocial care. * Arm II: Patients receive their institution's usual psychosocial care only. Quality of life, anxiety, and depression are assessed at baseline and then at 1, 2, and 3 weeks. Intervention helpfulness is assessed at 3 weeks. PROJECTED ACCRUAL: A total of 327 patients (approximately 163 per treatment arm) will be accrued for this study within 2 years.

Conditions

Interventions

TypeNameDescription
PROCEDUREpsychosocial assessment and care
PROCEDUREquality-of-life assessment

Timeline

Start date
2003-02-01
Primary completion
2005-04-01
Completion
2006-06-01
First posted
2003-04-09
Last updated
2013-05-30

Locations

12 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT00057733. Inclusion in this directory is not an endorsement.