CAncer, NUtrition and Taste - Validation of the CANUT-QVA Questionnaire on Eating Habits in Cancer Patients

NCT ID: NCT04235153

Last Updated: 2021-07-09

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 127 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2020-01-09
• Study Completion Date: 2020-03-12

Brief Summary

Cancer patients are at high risk of undernutrition, which is generally more pronounced for solid tumours (upper digestive tract, Ear Nose and Throat (ENT), bronchial tubes). This undernutrition leads to major weight loss and cachexia, and may represent the first sign of a call for a diagnosis of cancer. Cancer-related undernutrition is multi-factorial origins and has multiple consequences.

Chemotherapy treatments can induce various adverse effects in patients, including sensory disturbances at the beginning of treatment in addition to disturbances that may already be present before any treatment. The alteration of taste and odour, observed in 86% of patients, can induce a change in food preferences, promote the development of aversions, and therefore, lead to a significant reduction in the pleasure of eating. Loss of appetite, decreased food intake and the development of aversions to certain foods are situations experienced by a large proportion of patients treated with chemotherapy.

The assessment of taste disorders in patients treated with chemotherapy is established through the use of questionnaires, interviews and taste tests.

Changes in the perception and identification of salty, sweet, bitter and sour flavours are common in patients treated with chemotherapy.

As regards food products, patients report developing olfactory hypersensitivity mainly for food of animal origin, in particular for odours of fish, frying, cheese and eggs.

The CANUT project aims to study the effect of pathology and chemotherapy on gustatory and olfactory mechanisms, and in particular on interindividual differences in the perception and appreciation of food.

In order to monitor the evolution of patients' eating habits over time, the diet-related quality of life questionnaire (CANUT-QVA) was constructed from items selected from the Well-being related to Food questionnaire (WELLBFQ) after eliminating questions that were too general or expressed in terms of importance to use perception-related responses as a priority.

After this part, an evaluation of the 9 dimensions of the CANUT-QVA questionnaire will be performed.

Conditions

Hematologic Cancer; Undernutrition; Chemotherapy Effect; Taste Disorders; Chemotherapy-Induced Change; Olfactory Disorder

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Study Groups

Patients with solid or hematological cancer

All the patients complete the CANUT-QVA questionnaire

Evaluation of the 9 dimensions of the CANUT-QVA questionnaire

Intervention Type: OTHER

Evaluation of the contribution of a new questionnaire by patients with solid or hematological cancer according to 9 dimensions:

1. Making food

2. Place where the meals are eaten

3. Eating and drinking: Nutrition

4. Eating and drinking: The pleasure of tasting, chewing

5. Eating and drinking: Satiated, well being

6. Food preparation: Supply, choice, presentation

7. Eating and drinking: Feelings

8. After eating: heaviness, discomfort, hunger

9. Taste/Odour Problems to confirm the number and structure of factors obtained at the end of the pre-study and to remove redundant questions.

Interventions

Evaluation of the 9 dimensions of the CANUT-QVA questionnaire

Evaluation of the contribution of a new questionnaire by patients with solid or hematological cancer according to 9 dimensions:

1. Making food

2. Place where the meals are eaten

3. Eating and drinking: Nutrition

4. Eating and drinking: The pleasure of tasting, chewing

5. Eating and drinking: Satiated, well being

6. Food preparation: Supply, choice, presentation

7. Eating and drinking: Feelings

8. After eating: heaviness, discomfort, hunger

9. Taste/Odour Problems to confirm the number and structure of factors obtained at the end of the pre-study and to remove redundant questions.

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• Patient with solid or hematological cancer (any stage of disease and any treatment) diagnosed within 12 months of inclusion.
• Patient who does not object to participate in the trial
• Patient affiliated to a social security system

Exclusion Criteria

• Minor patient (age <18 years).
• Patient under trusteeship, curatorship or protective measures.
• Patient who has already completed the questionnaire.
• Patient not sufficiently able to speak French to answer the questionnaire

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Hospices Civils de Lyon

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Hospices Civils de Lyon, Groupement Hospitalier Lyon Sud, Service pneumologie

Pierre-Bénite, , France

Countries

France

Other Identifiers

69HCL19_0617

Identifier Type: -

Identifier Source: org_study_id