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Exercise for Fighting Oncology Repercussions After Treatment

Exercise for Fighting Oncology Repercussions After Treatment: the EFFORT Trial

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05980325
Acronym
EFFORT
Enrollment
45
Registered
2023-08-08
Start date
2025-01-08
Completion date
2026-07-01
Last updated
2024-12-06

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

Conditions

Neoplasms

Keywords

Neoplasms, Exercise Therapy, Side Effects, Cancer-related Fatigue, Quality of Life

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.

Interventions

BEHAVIORALNordic Walking

A 12-week Nordic Walking exercise programme supervised twice weekly

A 12-week water-based exercise training programme supervised twice weekly

A 12-week circuit-based exercise training programme supervised twice weekly

Sponsors

Col·legi de Fisioterapeutes de Catalunya
CollaboratorUNKNOWN
Ajuntament de Mataró
CollaboratorUNKNOWN
Universitat Pompeu Fabra
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Health-Related Quality of Life12 weeks from baselineHRQoL measured with the EORTC Quality of Life C30 questionnaire

Secondary

MeasureTime frameDescription
Cancer-related fatigue12 weeks from baselineCancer-related fatigue as measure with the Brief Fatigue Inventory
Cardiorespiratory fitness12 weeks from baselineA steady state cardiopulmonary exercise testing with breath-by-breath analysis and lactate measurement to determine submaximal cardiorespiratory fitness
Estimated one-repetition maximum12 weeks from baselineEstimated maximal muscle strength using a linear Encoder for two main muscle groups: i) chest and ii) quads
Lower limb muscle endurance12 weeks from baselineLower limb muscle endurance measured as the maximum number of sit-to-stand repetitions performed in 30 seconds
Functional capacity12 weeks from baselineWalking distance covered during a self-pace 6 minute walk test

Contacts

Primary ContactEsther Mur Gimeno, PhD
emur@tecnocampus.cat+34931696573
Backup ContactRaquel Sebio García, PhD
rsebio@tecnocampus.cat+34634787194

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026