RECRUITING

Exercise and Nutritional Prehabilitation for Head and Neck Cancer Patients

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Conditions

Head CancerNeck CancerSarcopeniaHead and Neck CancerExerciseNutritionalPrehabilitationHeadNeckCancer

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

This study examines the acceptability, feasibility, and safety in developing a prehabilitation program for head and neck cancer patients. The purpose of this research is to access the safety and acceptability of using a prehabilitation program before head and neck cancer surgery.

Official Title

Exercise and Nutritional Prehabilitation for Head and Neck Cancer Patients

Quick Facts

Study Start:2024-05-09
Study Completion:2025-12
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06722508

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. Age 18 years or older
  2. Willing and able to provide informed consent
  3. Able to understand and follow study procedures
  4. Stable medical condition
  1. 1. Prior treatment for head and neck cancer (surgery and/or radiation)
  2. 2. Acute or unstable cardiac conditions (unstable angina or symptomatic severe aortic stenosis)
  3. 3. American Society of Anesthesiologists physical status of 4 and 5
  4. 4. Disabling orthopedic or neuromuscular disease
  5. 5. Cardiac failure (New York Heart Association functional classes III and IV)
  6. 6. Severe chronic obstructive pulmonary disease
  7. 7. End-stage liver or kidney disease
  8. 8. Inability to swallow and/or feeding tube dependence
  9. 9. Any other comorbid medical, physical, and/or mental condition that contraindicates exercise or oral nutrition
  10. 10. Adults unable to consent
  11. 11. Age 17.99 or younger
  12. 12. Prisoners, pregnant women, or other vulnerable population

Contacts and Locations

Study Contact

Randev Sandhu CRC Supervisor, BS
CONTACT
9167342863
rssandhu@ucdavis.edu
Marianne Abouyared PI, MD
CONTACT
9167342801
mabouyared@ucdavis.edu

Principal Investigator

Marianne S Abouyared, MD
PRINCIPAL_INVESTIGATOR
University of California, Davis

Study Locations (Sites)

UC Davis Health
Sacramento, California, 95817
United States
UC Davis Medical Center
Sacramento, California, 95817
United States

Collaborators and Investigators

Sponsor: University of California, Davis

  • Marianne S Abouyared, MD, PRINCIPAL_INVESTIGATOR, University of California, Davis

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-05-09
Study Completion Date2025-12

Study Record Updates

Study Start Date2024-05-09
Study Completion Date2025-12

Terms related to this study

Keywords Provided by Researchers

  • Exercise
  • Nutritional
  • Prehabilitation
  • Head
  • Neck
  • Cancer

Additional Relevant MeSH Terms

  • Head Cancer
  • Neck Cancer
  • Sarcopenia
  • Head and Neck Cancer