Group-Mediated Cognitive Behavioral Resistance Exercise Intervention in Head and Neck Cancer Patients Undergoing Chemoradiation Treatment
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- STATUS
- Recruiting
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- End date
- Dec 31, 2024
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- participants needed
- 20
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- sponsor
- Ohio State University Comprehensive Cancer Center
Summary
This clinical trial examines a group-mediated cognitive behavioral resistance exercise intervention in head and neck cancer patients who are undergoing chemoradiation treatment. Chemoradiation is the established standard of care for locally advanced head and neck cancer patients. However, many head and neck cancer patients experience clinically meaningful declines in muscle mass, physical function, and quality of life during and following treatment. Resistance exercise has been shown to improve muscle mass, body composition, and physical function when integrated with appropriate standard of care nutritional counseling/supplementation. This trial may help researchers determine the important of integrating exercise interventions with routine cancer care.
Description
PRIMARY OBJECTIVES:
I. To determine the feasibility of implementing a group-mediated cognitive behavioral (GMCB) personalized resistance exercise (RE) intervention in head and neck cancer (HNCa) patients undergoing chemoradiation (CRT).
II. To examine the effects of GMCB RE intervention upon functional limitations, body composition, and quality of life (QOL) in HNCa patients undergoing CRT.
- OUTLINE
Patients undergo personalized resistance exercises over 1 hour daily. Patients receive dietary counseling over 60 minutes at week 1 and then over 15-30 minutes weekly for up to 6 weeks. Patients also receive group-based behavioral counseling twice weekly (BIW) in weeks 1-8, once a week (QW) in weeks 9-12, and then twice a month in weeks 13-24.
Details
| Condition | Locally Advanced Head and Neck Squamous Cell Carcinoma |
|---|---|
| Treatment | questionnaire administration, quality-of-life assessment, Resistance Training, Counseling, Dietary Counseling and Surveillance |
| Clinical Study Identifier | NCT04733495 |
| Sponsor | Ohio State University Comprehensive Cancer Center |
| Last Modified on | 22 March 2022 |
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