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Occupational therapy and nutritional pre-operative intervention in bone sarcoma cases- A Feasibility study

Multimodal prehabilitation in patients with bone sarcomas around knee joint- a feasibility study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/04/042236
Enrollment
30
Registered
2022-04-28
Start date
Unknown
Completion date
Unknown
Last updated
2025-05-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: C402- Malignant neoplasm of long bones of lower limb

Interventions

Intervention1: Multimodal prehabilitation including occupational therapy and nutritional intervention: Occupational therapy prehabilitation intervention will include- techniques to maintain positivie
and post operatively on completion of 1st, 2nd and 3rd month hence in total 3 times. Control Intervention1: NOT APPLICABLE: NOT APPLICABLE

Sponsors

Tata Memorial Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients with primary bone sarcomas of i.e., proximal tibia and distal end of femur Patients planned for limb salvage surgery i.e., endoprosthetic reconstruction. Before commencement of chemotherapy (3 weekly protocol, 4 cycles preoperatively and 4 cycles post operatively). Age group- 18-60 years old. Gender- Males and Females. Patients who are literate, able to read and understand Hindi or English language. Patients willing to follow-up to occupational therapy dept. for defined prehabilitation period.

Exclusion criteria

Exclusion criteria: Patients pre- operated for primary bone sarcomas of proximal end of tibia including endoprosthetic reconstruction. Secondary bone sarcomas cases (bone metastasis). Patients with disease progression Patients receiving chemotherapy outside Tata Memorial Hospital Patients with pathological fractures and distant metastasis and local recurrence. Presence of prior mental, psychiatric, cognitive impairment that precludes self-care.

Design outcomes

Primary

MeasureTime frame
Since this is a feasibility study we shall be mentioning the scores (Performance components, DASS-21, MULTIDIMENSIONAL FATIGUE INVENTORY 20, SUBJECTIVE GLOBAL ASSESSMENT, CANADIAN OCCUPATIONAL PERFORMANCE MEASURE), proportion, ranges of patients who complete assessments.Timepoint: Assessments will be conducted on following time points- baseline which will be done on one day before 1st chemotherapy administration, 1 day before 2nd, 3rd, 4th and 21st day after last i.e. 4th chemotherapy cycle. post operatively assessments will be done on completion of 1st, 2nd and 3rd month of surgery

Secondary

MeasureTime frame
NILTimepoint: NOT APPLICABLE

Countries

India

Contacts

Public ContactMahesh alias Vibhav M Sanzgiri

Tata Memorial Hospital

vagalmanjusha@yahoo.com9867552266

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026