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Clinical Trials/NCT01910753
NCT01910753
Terminated
Not Applicable

Feasibility Study: Physical Activity Program Associated Wtih Nutrition Therapeutic Education in Head and Neck Cancer Population Treating by Chemotherapy With or Without Radiotherapy.

University Hospital, Limoges2 sites in 1 country10 target enrollmentMay 2013
ConditionsNeck Cancer

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Neck Cancer
Sponsor
University Hospital, Limoges
Enrollment
10
Locations
2
Primary Endpoint
feasibility of the APA with a composite outcome measure
Status
Terminated
Last Updated
9 years ago

Overview

Brief Summary

The purpose of this study is to examine the feasibility of resistance training and physical functioning associated with nutrition therapeutic education in head and neck cancer patients, during their treatment (chemotherapy with or without radiotherapy).

Detailed Description

The loss of muscle mass (i.e., sarcopenia) has been identified as a negative prognosis descriptor, disregarding the type of cancer. It is also a predictive descriptor for treatment-related toxicity. Therefore it appears crucial to save muscle mass of patients, following an adequate physical training together with a personalised diet program. The latter point is of major importance as malnutrition concerns 45% patients having head and neck cancer cancer, who stop physical activity due to extreme tiredness and decrease of quality of life. In the present project, we plan a physical activity program that would be adapted to each patient, accompanied by the rethought diet over a 3-month period. The adapted physical activity (APA) is constituted of two aerobic stages and one resistance training stage per a week. The evaluation will then proceed at three different moments, namely (i) at T0 i.e., beginning of the program, (ii) at 3 months i.e., when the program will be stopped, and (iii) at 6 months i.e., three months after the program stop. This evaluation will include the success rate, the level of satisfaction, the physiological parameters (VO2max, muscle mass and strength, BMI) and quality of life.

Registry
clinicaltrials.gov
Start Date
May 2013
End Date
June 2015
Last Updated
9 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
University Hospital, Limoges
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Age\>18 years
  • Written informed consent provided before any study specific procedures
  • Consent to cooperate for clinical assessments
  • Affiliation to a social security regime or beneficiary of equivalent social protection
  • Performance status between 0 and 2
  • Squamous cell carcinoma of oral cavity, oropharynx or hypopharynx
  • Stage III - IV (T1-T4, N0-N3, M)(UICC 2002)
  • Indication of radiotherapy and chemotherapy post-operative or first-line metastatic chemotherapy or in inoperable condition
  • Ability to understand the nature, goal and study methodology

Exclusion Criteria

  • Prior neoadjuvant chemotherapy
  • timed vital capacity\< 70%
  • Presence of another severe pathology including:
  • severe or chronic cardiac, pulmonary, renal and/or hepatic insufficiencies
  • Cons-indication to physical activity practice, at discretion of the investigator
  • Patient under guardianship
  • Psychological, social, geographical, or familial reasons prohibiting physical activity and follow-up
  • Any other primary tumor during the last 5 years
  • Pregnant or nursing

Outcomes

Primary Outcomes

feasibility of the APA with a composite outcome measure

Time Frame: 3 months

The evaluation criteria for the PA program will be: * The success rate that will be reached if 80% of physical exercises will be performed by the patient, over the 3-month period, * The level of satisfaction that will be evaluated with questionnaires filled by the patient.

Secondary Outcomes

  • Evaluation of the personalised diet program and the therapeutic education with a composite outcome measure.(3 months)

Study Sites (2)

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