Pre- and Post-Operative Exercise Program in Upper Gastrointestinal Cancers

NCT03807518 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 72

Last updated 2021-03-09

No results posted yet for this study

Summary

Esophageal and gastric cancers are a considerable health burden. In the past 10 years the 5-year survival for both cancers has doubled. This is due to a number of factors including advances in neo adjuvant and adjuvant chemotherapy and radiotherapy. However, physical fitness significantly declines as a result of neo adjuvant an adjuvant therapy. From studies in other cancers it is known that peri operative training improves physical fitness, yet there is little research into its effects in those with upper gastrointestinal cancers. The aim of this study is to assess the effect of a pre-and post operative training program on patients with upper gastrointestinal cancers on their physical fitness and consequently their optimism, quality of life and post operative morbidity.

Conditions

  • Exercise Intervention

Interventions

BEHAVIORAL

Standard Exercise Program

Standard Exercise Program- Participants will be invited to take part in a structured home, supervised, or both, exercise program while undergoing neo adjuvant therapy and for a six week period when deemed fit post surgery.

Sponsors & Collaborators

  • Beaumont Hospital

    collaborator OTHER
  • Mercy University Hospital, Cork, Ireland

    collaborator OTHER
  • Dublin City University

    collaborator OTHER
  • Royal College of Surgeons, Ireland

    lead OTHER

Principal Investigators

  • William Robb, MB,BCh,BAO,BA,FRCSI,MD · Beaumont Hospital Dublin

  • Noel McCaffrey, MB,BCh,BAO,BSc,MSc · Dublin City University

  • Thomas Murphy, MB,BCh,BAO,FRCSI · Mercy University Hospital, Cork

  • Jarlath Bolger, MB,BCh,BAO,MD · Beaumont Hospital

  • Pamela Gallagher, Professor of Psychology · Dublin City University

  • Claire Timon, BSc,PhD · University College Dublin

  • Jan Sorensen, MSc, MA · Royal College of Surgeons, Ireland

Study Design

Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-03-01
Primary Completion
2020-12-19
Completion
2021-03-01

Countries

  • Ireland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03807518 on ClinicalTrials.gov