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Clinical Trial Summary

The study includes patients with tumors of the oropharynx, larynx and hypopharynx scheduled to receive radiotherapy with curative intent (+/- chemotherapy). The patients will be randomized into either an intervention group (performing a preventive physical activity protocol before and during radiotherapy) or a control group not performing a specified physical exercise protocol. All patients will be in contact with with a speech language pathologist or a physical therapist weekly during radiotherapy. The study is expected to improve physical function and quality of life during and after oncologic treatment


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05432297
Study type Interventional
Source Sahlgrenska University Hospital, Sweden
Contact Lisa Tuomi, PhD
Phone +46313421000
Email tuomi.lisa@gu.se
Status Recruiting
Phase N/A
Start date January 2, 2023
Completion date December 2031

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