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Completed

NCT Number: NCT01332682

Resistance Training and Physical Functioning in Head and Neck Cancer Patients

The purpose of this feasibility study is to examine the safety and effect of resistance training on muscle strength, lean body mass, physical functioning, fatigue, and quality of life in head and neck cancer patients receiving radiation therapy.

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Key information

Age range

18 year–90 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Southern Illinois University School of Medicine

Springfield, Illinois, 62702, United States

About this study

Head and neck cancer (HNCa) patients often lose significant body weight and lean mass which is associated with higher mortality, greater fatigue, poorer quality of life, and reduced physical functioning. Because nutritional supplementation may not consistently improve lean body mass, resistance training may be beneficial. HNCa patients experience unique side effects that impact nutritional status, limiting generalization of exercise intervention study results in other cancer types to HNCa patients. Therefore, 44 HNCa patients will be enrolled in a randomized controlled trial with the following study aims:

Primary study aim: Because this pilot proposal is among the first to attempt a randomized controlled exercise trial in HNCa patients, the primary study aim examines safety and feasibility (e.g., study acceptance, recruitment, intervention process evaluation, adherence, adverse events, retention). The investigators hypothesize that study procedures will require minor alterations in future studies.

Secondary study aim #1: Because effect sizes are necessary for planning efficacy trials, the proposal will compare the effect of a 12-week resistance training plus nutritional counseling intervention versus nutritional counseling alone on muscle strength, lean body mass, physical functioning, fatigue, and quality of life in HNCa patients receiving radiation with or without chemotherapy. The investigators hypothesize that patients receiving resistance training with nutritional counseling will demonstrate greater improvements in the outcomes when compared with participants receiving nutritional counseling alone.

Secondary study aim #2: To enhance adherence in future intervention trials, this proposal will determine resistance training and nutritional adherence rates and associated factors among HNCa patients using attendance records, exercise logs, diet records, self-administered survey, and medical record review. The investigators hypothesize that adherence rates will be lower than that of other cancer populations with correlates including demographic, medical, and psychosocial factors.

Assessments will occur at baseline (first week of radiation), week 6 (mid-intervention), and week 12 (post-intervention). Qualitative and quantitative (e.g., rates, 95% confidence intervals) will assess feasibility and mixed model ANOVA will examine group differences. This information is critical for the design of future resistance training efficacy trials in HNCa patients to prevent lean body mass loss in HNCa patients, potentially reducing mortality, minimizing fatigue, and improving physical functioning and quality of life.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • cancer of the oral cavity, pharynx, larynx, nasal cavity/sinuses, or salivary gland
  • ≥ 18 years of age
  • English speaking
  • radiation therapy planned or underway < 1 week, and
  • able to stand

Exclusion criteria

  • dementia or organic brain syndrome
  • severe emotional distress
  • active schizophrenia
  • quadriplegia or loss of use of limbs or torso
  • tendon rupture
  • muscle tear
  • cancer recurrence
  • another diagnoses of cancer in the past 5 years, and
  • oncologist refuses to allow screening for possible study participation

Treatment and study plan

Nutrition counseling

Behavioral

Patients will meet once per week with dietitian for the first 6 weeks in 60 minute sessions. Dietitian will telephone each patient weekly for the final 6 weeks of counseling and support.

Other names: nutrition

Resistance Training and Nutrition Counseling

Behavioral

Patient will meet with an exercise specialist once per week for the first 6 weeks. Patient will receive guidance in a safe and appropriate exercise regimen based on specific medical history and preference. An exercise specialist will telephone weekly for consultation and support once per week for the final 6 weeks. Also, patient will meet once per week with dietitian for the first 6 weeks in 60 minute sessions. Dietitian will telephone each patient weekly for the final 6 weeks of counseling and support.

Primary outcomes

  1. safety of head and neck cancer patients

    Time frame: daily (up to 12 weeks)

    adverse events

Secondary outcomes

  1. change in muscle strength

    Time frame: baseline, week 6, and week 12

    dynamometer measurement

  2. Number of patients who adhere to cohort activity schedule

    Time frame: baseline, week 6, and week 12

    completion of exercise or diet recommendations

  3. change in lean body mass

    Time frame: baseline, week 6, week 12

    bioelectrical impedence

  4. change in physical functioning

    Time frame: baseline, week 6, week 12

    physical performance by doing a semi-tandem, tandem, or side by side stance with the feet, an 8 foot walk time, and 5 chair rise and sits

  5. change in fatigue level

    Time frame: baseline, week 6, week 12

    13-item Functional Assessment of Cancer Therapy-Fatigue scale

  6. change in quality of life

    Time frame: baseline, week 6, week 12

    37-item Functional Assessment of Cancer Therapy-Head and Neck scale

  7. Number of head and neck cancer patients recruited to participate

    Time frame: up to 16 months

    to test the feasibility of a randomized controlled exercise trial in head and neck cancer patients receiving radiation therapy

Sponsors and collaborators

Lead sponsor

University of Alabama at Birmingham

Other

Registry information

Important dates

Study start
2009
Primary completion
2010
Study completion
2012
First posted
Apr 11, 2011
Registry last updated
Oct 18, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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