A comparative study between two techniques to improve range of movement in patients after head and neck cancer surgery
Not Applicable
- Conditions
- Health Condition 1: null- patients with Head and Neck cancer who underwent Modified Radical Neck Dissection
- Registration Number
- CTRI/2017/03/008072
- Lead Sponsor
- Anmol Thomas
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 90
Inclusion Criteria
all genders, age 30-65 years, people who underwent modified radical neck dissection post surgical day 3-5 onwards
Exclusion Criteria
previous fracture/ surgery to the shoulder, rotator cuff injuries, recurrent shoulder dislocations
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain- Visual analogue scale (VAS) <br/ ><br>Range of motion- GoniometerTimepoint: VAS score after 10 days <br/ ><br>Range of motion measure after 10 days
- Secondary Outcome Measures
Name Time Method Global rating of change scaleTimepoint: Global rating of change scale score after 10 days of treatment