Physical Activity Program and Nutrition Therapeutic Education During Treatment of Head and Neck Cancer Population (APANVADS)
Primary Purpose
Neck Cancer
Status
Terminated
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
APA
Sponsored by
About this trial
This is an interventional prevention trial for Neck Cancer focused on measuring Head and neck cancer,, physical activity,, nutrition therapeutic education
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
Sites / Locations
- CHU LIMOGES - Explorations Fonctionnelles Respiratoires
- CHU LIMOGES - Oncologie
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
APA
Arm Description
Patient with neck cancer and accepting the physical activity program .
Outcomes
Primary Outcome Measures
feasibility of the APA with a composite outcome measure
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 Outcome Measures
Evaluation of the personalised diet program and the therapeutic education with a composite outcome measure.
The evaluation criteria for the personalised diet program and the therapeutic education will be:
The success rate that will be reached if 80% of requirements will be addressed by the patient,
The level of satisfaction that will be evaluated with questionnaires filled by the patient.
Full Information
NCT ID
NCT01910753
First Posted
July 22, 2013
Last Updated
September 6, 2016
Sponsor
University Hospital, Limoges
1. Study Identification
Unique Protocol Identification Number
NCT01910753
Brief Title
Physical Activity Program and Nutrition Therapeutic Education During Treatment of Head and Neck Cancer Population
Acronym
APANVADS
Official Title
Feasibility Study: Physical Activity Program Associated Wtih Nutrition Therapeutic Education in Head and Neck Cancer Population Treating by Chemotherapy With or Without Radiotherapy.
Study Type
Interventional
2. Study Status
Record Verification Date
September 2016
Overall Recruitment Status
Terminated
Why Stopped
Not enough patients
Study Start Date
May 2013 (undefined)
Primary Completion Date
June 2015 (Actual)
Study Completion Date
June 2015 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Limoges
4. Oversight
Data Monitoring Committee
No
5. Study Description
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Neck Cancer
Keywords
Head and neck cancer,, physical activity,, nutrition therapeutic education
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
10 (Actual)
8. Arms, Groups, and Interventions
Arm Title
APA
Arm Type
Experimental
Arm Description
Patient with neck cancer and accepting the physical activity program .
Intervention Type
Procedure
Intervention Name(s)
APA
Intervention Description
A 3-month program for physical activity and diet education will be followed. An exercise specialist will supervise patients twice per week, during the first six weeks. They will also follow nutrition counselling and therapeutic education by a dietician once per week. During the last six weeks, they will just follow a guide for safe and appropriate exercise regimen. The dietician will call patient weekly during this final period.
Primary Outcome Measure Information:
Title
feasibility of the APA with a composite outcome measure
Description
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.
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Evaluation of the personalised diet program and the therapeutic education with a composite outcome measure.
Description
The evaluation criteria for the personalised diet program and the therapeutic education will be:
The success rate that will be reached if 80% of requirements will be addressed by the patient,
The level of satisfaction that will be evaluated with questionnaires filled by the patient.
Time Frame
3 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
FRANCOIS Vincent, MD
Organizational Affiliation
Limoges UH
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Sabrina FALKOWSKI, MD
Organizational Affiliation
CHU LIMOGES - Oncologie
Official's Role
Principal Investigator
Facility Information:
Facility Name
CHU LIMOGES - Explorations Fonctionnelles Respiratoires
City
Limoges
ZIP/Postal Code
87042
Country
France
Facility Name
CHU LIMOGES - Oncologie
City
Limoges
ZIP/Postal Code
870
Country
France
12. IPD Sharing Statement
Learn more about this trial
Physical Activity Program and Nutrition Therapeutic Education During Treatment of Head and Neck Cancer Population
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