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Study to evaluate the impact of structured prehabilitation program on post operative outcomes in patients undergoing major cancer surgeries Prehabilitation

A Randomised Control Study on Prehabilitation prior to major cancer surgeries - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/06/112814
Enrollment
50
Registered
2026-06-16
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-22

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

Conditions

Health Condition 1: C249- Malignant neoplasm of biliary tract, unspecified Health Condition 2: C189- Malignant neoplasm of colon, unspecified Health Condition 3: C159- Malignant neoplasm of esophagus, unspecified Health Condition 4: C23- Malignant neoplasm of gallbladder Health Condition 5: C399- Malignant neoplasm of lower respiratory tract, part unspecified Health Condition 6: C259- Malignant neoplasm of pancreas, unspecified Health Condition 7: C20- Malignant neoplasm of rectum Health Conditi

Interventions

Intervention1: exercise, dietary modifications, psychological support and addiction cessation in cancer patients atleast 4 weeks prior to surgery: cancer patients in study group will undergo structure

Sponsors

ARMY HOSPITAL RESEARCH AND REFERRAL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients scheduled for major cancer surgeries (thoracic, abdominal etc) 2. Between the age of 18 to 80 years (both inclusive)

Exclusion criteria

Exclusion criteria: 1. Patients undergoing emergency cancer surgeries. 2. Severe co morbid conditions limiting participation in prehabilitation 3. Cognitive impairment affecting consent or adherence

Design outcomes

Primary

MeasureTime frame
To assess role of prehabilitation in reducing post operative complications in patients undergoing major cancer surgeriesTimepoint: 30 days post surgery

Secondary

MeasureTime frame
To evaluate the role of prehabilitation on length of hospital stay, readmission rates, improvement in nutritional status, improvement in functional statusTimepoint: 30 days post surgery

Countries

India

Contacts

Public ContactAMIT AGRAWAL

ARMY HOSPITAL RESEARCH AND REFERRAL

majoramitagrawal@gmail.com9971664222

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 29, 2026