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NCT06079697Completed

An Exercise Prehabilitation Intervention for Improving Mobility and Recovery Outcomes in Patients Undergoing Head and Neck Cancer Surgery

The Effect of Exercise Prehabilitation on Post-Operative Recovery After Head and Neck Cancer Surgery

Source: ClinicalTrials.gov · Last updated 12 Dec 2025

Brief summary (registry, in English)

This clinical trial evaluates a prehabilitation exercise intervention for improving mobility and recovery outcomes in patients undergoing surgery for head and neck cancer. Prehabilitation focuses on optimizing health before surgery in order to improve outcomes after surgery. Prehabilitation may include aspects of nutrition, exercise, mental health, or a combination of these. Exercise has been proven to improve anxiety, depression, fatigue, health related quality of life, and physical function among patients undergoing cancer treatment, as well as cancer survivors. The prehabilitation exercise intervention being studied includes a daily walking program, sit-to-stand training, and standing therapeutic exercises before patients undergo surgery. Receiving this prehabilitation exercise intervention prior to surgery may improve mobility and recovery outcomes in patients after surgery for head and neck cancer.

Status (registry)
Completed
Study type
Interventional
Enrollment
52 (actual)
First submitted
28 Sept 2023
Start date
1 Feb 2024
Primary completion date
15 Jul 2025
Lead sponsor
OHSU Knight Cancer Institute
NCT number
NCT06079697

What you commit to

  • Study type: Interventional
  • Participants enrolled: 52
  • From 1 Feb 2024 to the primary completion date, 15 Jul 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Social or psychiatric conditions that may interfere with compliance
  • Further exclusion criteria may be applied due to conditions that may impact the ability to safely exercise as well as utilize the Fitbit devices:
  • Symptoms of or ongoing work-up for unstable angina, uncontrolled tachyarrhythmias, decompensated heart failure, severe aortic stenosis, hypertrophic obstructive cardiomyopathy, uncontrolled hypertension (HTN), uncontrolled pulmonary HTN or uncontrolled asthma
  • History of chest pain, dizziness or syncope with exercise

Other

  • Non-English speaking
  • Planned postoperative admission to the intensive care unit (ICU)
  • Bony metastases to the spine or extremities
  • Falls in the last year
  • Cognitive impairments limiting safety or ability to use technology
  • Impaired mobility requiring the use of assistive devices, such as use of a walker or wheelchair at baseline
  • Isolation precautions, as they would not be allowed to ambulate on a patient floor post-operatively

Who the study is looking for

  • Older than 18 years of age and younger than 89 years of age. Both men and women and members of all races and ethnic groups may be included
  • Planned to undergo major head and neck cancer surgery with free tissue transfer reconstruction at Oregon Health and Science University (OHSU) with the Department of Otolaryngology-Head and Neck Surgery with an expected length of stay (LOS) of 3 days or more
  • Ability to understand and the willingness to sign a written informed consent document

Age in the registry: 18 years to 89 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
OHSU Knight Cancer Institute
Coordinator of this site? Confirm its status
PortlandUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.