Actively Recruiting

Phase 1
Phase 2
Age: 65Years +
All Genders
NCT06412510

Prehabilitation for EOC, Fallopian Tube, Primary Peritoneal Carcinoma and Pancreatic Cancer w/ NACT

Led by Case Comprehensive Cancer Center · Updated on 2026-03-18

22

Participants Needed

1

Research Sites

51 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The purpose of this study is to see whether participants who are assigned to a multimodal prehabilitation intervention during chemotherapy are able to adhere with exercise and nutrition program to prepare for their cancer surgery.

CONDITIONS

Official Title

Prehabilitation for EOC, Fallopian Tube, Primary Peritoneal Carcinoma and Pancreatic Cancer w/ NACT

Who Can Participate

Age: 65Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 65 and older
  • Diagnosis of advanced (Stage III or IV) epithelial ovarian, fallopian tube, or primary peritoneal carcinoma
  • Diagnosis of pancreatic adenocarcinoma (Stage I, II, or III) undergoing neoadjuvant chemotherapy
  • Diagnosis of locally advanced esophageal cancer undergoing neoadjuvant chemotherapy
  • Diagnosis of locally advanced muscle invasive bladder cancer undergoing neoadjuvant chemotherapy
Not Eligible

You will not qualify if you...

  • Life expectancy less than 3 months as determined by the treating physician
  • Unable to provide informed consent
  • Wheelchair bound or physically immobile
  • Severe cardiopulmonary disease defined as NYHA class III or IV
  • Malignant bowel obstruction requiring surgery or nutritional support by enteral or parenteral nutrition
  • Any other condition that places the patient at higher risk or burden or is not in the patient's best interest to participate

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Cleveland Clinic Taussig Cancer institute, Case Comprehensive Cancer Center

Cleveland, Ohio, United States, 44195

Actively Recruiting

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Research Team

M

Mariam AlHilli, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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