THE EFFECTIVENESS OF PRO SELF PAIN CONTROL AND GUIDED IMAGERY COMBINATION ON PAIN REDUCTION IN BREAST CANCER PATIENTS IN THE OUTPATIENT UNIT HASANUDDIN UNIVERSITY HOSPITA
Phase 2
- Registration Number
- TCTR20230923003
- Lead Sponsor
- There is no funding
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending (Not yet recruiting)
- Sex
- Female
- Target Recruitment
- 75
Inclusion Criteria
(1) Patients with a diagnosis of breast cancer stage 3-4, (2) Aged 18-59 years old and cooperative (able to respond and communicate with officers), (3) Patients who experience pain, (4) Using analgesics or chemotherapy, (5) Patients with breast cancer sores, (6) Able to write, read, speak Indonesian and operate a cell phone.
Exclusion Criteria
(1) Cancer metastases to the hearing organ, (2) Patients with Post Op Mastectomy/Lumpectomy breast injury, (3) Patients receiving radiation therapy, (4) Patients with special needs according to the level of severity, (5) Patients on psychotropic or antipsychotic drugs
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Reduction of pain intensity 3 Months Numeric Rating Scale
- Secondary Outcome Measures
Name Time Method Secondary outcomes included location of pain, duration of pain, type of pain, when pain was worse, type and dose of analgesic medication, what nonpharmacologic techniques were practiced 3 Months Pain Diary,Secondary outcomes include whether the combined Pro self-pain control and guided imagery intervention is better than the single Pro self-pain control and guided imagery intervention. 3 Months Results of data analysis