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Clinical Trials/NCT05980325
NCT05980325
Not yet recruiting
Not Applicable

Exercise for Fighting Oncology Repercussions After Treatment: the EFFORT Trial

Universitat Pompeu Fabra0 sites45 target enrollmentJanuary 8, 2025
ConditionsNeoplasms

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Neoplasms
Sponsor
Universitat Pompeu Fabra
Enrollment
45
Primary Endpoint
Health-Related Quality of Life
Status
Not yet recruiting
Last Updated
last year

Overview

Brief Summary

Cancer survival rates are currently on the verge of 70% at 5 years since diagnosis. Recent improvements in main cancer therapies including chemotherapy, radiotherapy, surgery and immunotherapy as well as developments of new biological therapies have significantly improved survival rates but unfortunately, cancer-related side effects continue to affect many patients even years after completion of main treatments. Exercise has been shown to not only ameliorate cancer-related effects before, during and after treatment but also improve disease-free and overall survival rates by decreasing risk factors associated with cancer risk and improving resilience to treatment. In this non-randomised, three-arm study, we aim to assess the effects of three forms of exercise (i.e: Nordic Walking, Aquatic Exercise and Functional Exercise) on physical performance, cancer-related fatigue, health-related quality of life and cancer-specific symptoms in a wide range of cancer survivors.

Registry
clinicaltrials.gov
Start Date
January 8, 2025
End Date
July 1, 2026
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Raquel Sebio

Senior Lecturer

Universitat Pompeu Fabra

Eligibility Criteria

Inclusion Criteria

  • Adults diagnosed with cancer
  • Completion of any cancer therapy in the previous 3 months with the exception of hormonal therapy
  • Patients living within the Maresme Area
  • No contraindications for exercise (oncology clearance or Physical Activity Readiness Questionnaire negative)

Exclusion Criteria

  • Patients with any neurologic, cognitive or musculoskeletal impairments that prevent them to engage in any assessment test or exercise modality.
  • Patients with unstable cardiac, respiratory or metabolic diseases
  • Unable to speak or read Catalan or Spanish

Outcomes

Primary Outcomes

Health-Related Quality of Life

Time Frame: 12 weeks from baseline

HRQoL measured with the EORTC Quality of Life C30 questionnaire

Secondary Outcomes

  • Estimated one-repetition maximum(12 weeks from baseline)
  • Lower limb muscle endurance(12 weeks from baseline)
  • Functional capacity(12 weeks from baseline)
  • Cancer-related fatigue(12 weeks from baseline)
  • Cardiorespiratory fitness(12 weeks from baseline)

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