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NCT07838090Not yet recruiting

Resistance Training and Creatine Supplementation for Head and Neck Cancer

Pilot Randomized Trial Evaluating Resistance Exercise Training and Creatine Supplementation in Individuals Treated for Head and Neck Cancer

Source: ClinicalTrials.gov · Last updated 6 Oct 2026

Brief summary (registry, in English)

The study will examine a 10-week resistance training program, with or without creatine monohydrate supplementation, in adult survivors of head and neck cancer. Participants will undergo screening and complete study assessments before and after the training period and at a follow-up evaluation. The study will evaluate feasibility, safety, body composition, physical function, cancer-related fatigue, quality of life, and symptom burden in this population.

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
30 (estimated)
First submitted
31 Aug 2026
Start date
15 Nov 2026
Primary completion date
15 Sept 2028
Lead sponsor
Medical University of South Carolina
NCT number
NCT07838090

What you commit to

  • Study type: Interventional
  • Planned participants: 30
  • From 15 Nov 2026 to the primary completion date, 15 Sept 2028
  • 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

  • Cognitive, psychiatric, or neurologic conditions that would impair ability to consent or adhere to study procedures.
  • Pre-existing renal impairment.

Other

  • Current participation in structured resistance training 2 or more days per week within the past 6 months.
  • Current use of creatine supplements, defined as consistently taking creatine more than 2 days per week for the past 6 months.

Who the study is looking for

  • Age 18 years or older.
  • Diagnosis of head and neck cancer (AJCC stages I-IV).
  • Completed curative-intent primary treatment, including surgery, radiation, chemotherapy, or combination treatment, within the past 1 to 3 months.
  • Clearance to engage in moderate-intensity exercise based on the American College of Sports Medicine (ACSM) Preparticipation Screening Guidelines.
  • Willingness and ability to participate in both in-person and/or virtual supervised exercise sessions.
  • Willingness to adhere to the supplementation regimen throughout the study.
  • English-speaking and able to understand study instructions and complete questionnaires.
  • Access to internet for remotely supervised exercise sessions.
  • Availability for the full 10-week intervention and post-intervention assessments.

Age in the registry: 18 years to - · 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
Medical University of South Carolina
Coordinator of this site? Confirm its status
CharlestonUnited StatesUnknown status

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