A trial to study the impact of two educational interventions on the relief of symptoms after operation in breast cancer patients.
Phase 3
- Conditions
- Health Condition 1: null- Pre and Post breast surgery patients
- Registration Number
- CTRI/2012/09/002957
- Lead Sponsor
- Department of Biotechnology
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 300
Inclusion Criteria
Female
Biopsy proven breast cancer patients
Scheduled to receive breast surgery
Exclusion Criteria
Male
Any Musculo-skeletal disorder
Any physical disability
Any mobility problem
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Percentage of patients developing Shoulder dysfunction. <br/ ><br>Percentage of patients developing lymphedema. <br/ ><br>Percentage of patients adhering to nutritional guidelines/diet chartsTimepoint: First follow up at 1 month, then at 3 months and then at 6 months in surgery OPD.
- Secondary Outcome Measures
Name Time Method illTimepoint: NA