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Recruiting NCT05988060

Physical Exercise for Patients With Head and Neck Cancer

Trial Parameters

Condition Head and Neck Cancer
Sponsor Institute Verbeeten
Study Type INTERVENTIONAL
Phase N/A
Enrollment 112
Sex ALL
Min Age 18 Years
Max Age N/A
Start Date 2022-11-09
Completion 2025-11-09
Interventions
Experimental Intervention

Brief Summary

The goal of this trial within cohorts study is to determine and compare physical performance, muscle strength, fatigue, quality of life, body composition, nutritional status, physical activity, treatment tolerability of radiotherapy (RT), chemoradiation (CRT) or bioradiation (BRT), and healthcare related costs in patients with head and neck cancer (HNC) with and without a 10 week physical exercise intervention (PEI) during RT, CRT or BRT ((C/B)RT). Patients who were randomized in the PEI group and accepted the invitation to undergo the experimental intervention receive a PEI twice a week for 10 weeks. The PEI will be executed 6 to 7 weeks during and 3 to 4 weeks after (C/B)RT. Researchers will compare patients who undergo the PEI with patients who did not undergo the PEI to see if there is difference in physical performance, muscle strength, fatigue, Quality of Life, body composition, nutritional status, physical activity, treatment tolerability of (C/B)RT , and healthcare related costs in patients with Head and Neck Cancer (HNC) with and without a 10 week Physical Exercise Intervention (PEI) during (C/B)RT).

Eligibility Criteria

Inclusion Criteria: 1. patients with HNC who are scheduled for (C/B)RT, 2. ≥18 years of age, 3. sufficient Dutch writing and reading skills, 4. a Karnofsky performance status (KPS) \>60, 5. able to walk ≥60m without a mobility aid, and 6. no contraindication for physical activity as measured with the physical activity readiness questionnaire (PAR-Q). Exclusion Criteria: 1. recurrence of HNC and/or 2. secondary HNC.

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