Clinical trial · Interventional
Physical Activity Program and Nutrition Therapeutic Education During Treatment of Head and Neck Cancer Population
Feasibility Study: Physical Activity Program Associated Wtih Nutrition Therapeutic Education in Head and Neck Cancer Population Treating by Chemotherapy With or Without Radiotherapy.
NCT01910753CI-TRIAL-00023776APANVADSterminatedN/AClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Why stopped (as posted): Not enough patients
Summary
Brief summary (as posted)
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).
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Neck Cancer | Malignant Neck Neoplasm | ALIAS | 0.90 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| APA | Procedure | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- APA
- description
- Patient with neck cancer and accepting the physical activity program .
- interventionNames
- Procedure: APA
Primary outcomes (1)
- measure
- feasibility of the APA with a composite outcome measure
- timeFrame
- 3 months
- 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.
Secondary outcomes (1)
- measure
- Evaluation of the personalised diet program and the therapeutic education with a composite outcome measure.
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
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
References
Publications (0)
Data not yet available
No reference posted for this study.