Comparison of designed pain management program and internal exposure on pain experienced in breast cancer patients
Not Applicable
- Conditions
- Patients with breast cancer who suffer from pain.
- Registration Number
- IRCT20220903055860N1
- Lead Sponsor
- The University of Isfahan
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 45
Inclusion Criteria
Breast cancer diagnosis
Receive chemotherapy
experience pain
Agreeing to participate in the research
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain experienced. Timepoint: Before intervention, immediately after intervention, 1 month after intervention. Method of measurement: Brief pain intensity questionnaire (Klind, 1991).
- Secondary Outcome Measures
Name Time Method ife expectancy. Timepoint: Before intervention, immediately after intervention, 1 month after intervention. Method of measurement: Life expectancy questionnaire of Snyder, Harris and Anderson (1991).