Evaluating function after surgery in Sarcoma patients as reported by the patient
Not Applicable
- Conditions
- Health Condition 1: C499- Malignant neoplasm of connective and soft tissue, unspecifiedHealth Condition 2: C402- Malignant neoplasm of long bones of lower limbHealth Condition 3: C400- Malignant neoplasm of scapula andlong bones of upper limb
- Registration Number
- CTRI/2023/01/048973
- Lead Sponsor
- Aarhus Sarcoma Centre
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Age >18 years
2.Treated surgically with curative intent for lower extremity bone or soft tissue sarcoma with a minimum period of 6 months post-surgery, to minimise early post treatment fluctuation in physical abilities
3.Ability to communicate in Hindi.
4.Ability to give a valid written informed consent.
Exclusion Criteria
1.Patients with impaired or challenged communication
2. Patients with unstable medical, oncologic or other emergencies
3.Patients being treated with palliative intent or best supportive care
4.Patients presenting with local or systemic recurrence at the time of evaluation
5.Patients presenting with active post-operative infection
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Comparison between PROMIS, EORTC QLQ-C30, MSTS and TESS will be done by assessing responder burden, correlation between scores and floor/ceiling effectsTimepoint: Minimum period of 6 months post-surgery
- Secondary Outcome Measures
Name Time Method oneTimepoint: Minimum period of 6 months post-surgery