Effectiveness of video based educational program on cancer fatigue among patients with breast cancer
Phase 1
- Conditions
- Health Condition 1: C509- Malignant neoplasm of breast of unspecified site
- Registration Number
- CTRI/2024/01/061583
- Lead Sponsor
- on Sponsorship
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients
-having age above 18 years and diagnosed breast cancer.
-receiving chemotherapy and completed at least one cycle of their chemotherapy
-willing to participate in the study.
-can able to understand and communicate in Hindi or English.
Exclusion Criteria
Patients
-with a history of psychiatric or neurological disorders that may affect fatigue perception (e.g., depression, anxiety, sleep disorders etc.)
-with hearing or visual impairments that may interfere with the comprehension of the video-based educational program.
-diagnosed with secondary metastatic breast cancer.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Fatigue level of the patients with breast cancer who have completed at least one cycle of chemotherapy will be assessed before and after of video based intervention through VAS-F fatigue scale.Timepoint: fatigue level will be assessed immediately after collecting baseline data ( 0 days) and after 1 month of giving the videobased intervention.
- Secondary Outcome Measures
Name Time Method ot ApplicableTimepoint: Not Applicable