ACTIVE_NOT_RECRUITING

The ENHANCE Study: Exercise and Nutrition in Head And Neck CancEr Survivors

Conditions

Oral Cavity Cancer Oropharynx Cancer Hypopharynx Cancer Larynx Cancer

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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

The purpose of the study is to design a physical activity and dietary intervention for head and neck cancer patients.

Official Title

The ENHANCE Study: Exercise and Nutrition in Head And Neck CancEr Survivors: A Randomized Clinical Trial

Quick Facts

Study Start:2023-04-06

Study Completion:2026-07

Study Type:Not specified

Phase:Not Applicable

Enrollment:Not specified

Status:ACTIVE_NOT_RECRUITING

Study ID

NCT05798780

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 Criteria	Exclusion Criteria
* \>18 years old * Newly diagnosed tumors of the oral cavity, oropharynx, hypopharynx, or larynx * No documented or observable psychiatric or neurological disorders that would interfere with study participation (e.g., dementia, psychosis) * Able to speak and read English * Able to consume food orally * Willing to consume an alternative Mediterranean diet * Scheduled to receive treatment with radiation or chemoradiation * Screened via the Physical Activity Readiness Questionnaire (PAR-Q+) with medical clearance of treating physicians, as necessary * Able to provide informed consent	* Women who are pregnant * Head and Neck Cancer not the primary diagnosis * Patients scheduled to receive surgery * Patients on enteral or parental nutrition

Inclusion Criteria

Exclusion Criteria

* \>18 years old
* Newly diagnosed tumors of the oral cavity, oropharynx, hypopharynx, or larynx
* No documented or observable psychiatric or neurological disorders that would interfere with study participation (e.g., dementia, psychosis)
* Able to speak and read English
* Able to consume food orally
* Willing to consume an alternative Mediterranean diet
* Scheduled to receive treatment with radiation or chemoradiation
* Screened via the Physical Activity Readiness Questionnaire (PAR-Q+) with medical clearance of treating physicians, as necessary
* Able to provide informed consent

* Women who are pregnant
* Head and Neck Cancer not the primary diagnosis
* Patients scheduled to receive surgery
* Patients on enteral or parental nutrition

Contacts and Locations

Principal Investigator

Sylvia Crowder, PhD

PRINCIPAL_INVESTIGATOR

Moffitt Cancer Center

Study Locations (Sites)

Moffitt Cancer Center

Tampa, Florida, 33612

United States

Collaborators and Investigators

Sponsor: H. Lee Moffitt Cancer Center and Research Institute

Sylvia Crowder, PhD, PRINCIPAL_INVESTIGATOR, Moffitt Cancer Center

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 Date2023-04-06

Study Completion Date2026-07

Study Record Updates

Study Start Date2023-04-06

Study Completion Date2026-07

Terms related to this study

Additional Relevant MeSH Terms

Oral Cavity Cancer
Oropharynx Cancer
Hypopharynx Cancer
Larynx Cancer