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New Food Solutions for Cancer Patients

Oncofood: New Food Solutions for Cancer Patients

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04302792
Acronym
Oncofood
Enrollment
88
Registered
2020-03-10
Start date
2020-06-09
Completion date
2020-12-31
Last updated
2021-06-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cancer Patients, Food Selection, Taste Disorders

Keywords

taste & smell alterations, texture-modified foods, taste-optimised foods, cancer patients

Brief summary

The ONCOFOOD project aims to design and develop new innovative food solutions for cancer patients, taking into account not only their nutritional requirements but also their sensory changes, promoting eating pleasure and preventing malnutrition. Research involving cancer patients but also their families and health care professionals is a key element of this approach to ensure the success of the developed products for the target group.

Detailed description

The study will be divided into three stages: in Stage 1, individual interviews will be conducted with present and past cancer patients, focus groups with families/care givers of cancer patients and health care professionals (cancer specialist nurses, clinical and medical oncologists, speech and language therapists, dietitians, oncology social workers and counselors). The interviews will help collect data and gain understanding on the needs of cancer patients, barriers to current food proposals and expectations from new solutions. In subsequent stages, semi-quantitative studies will be conducted with cancer patients that require texture-modified foods (Stage 2) and patients with taste & smell alterations (Stage 3). Patients will be required to evaluate texture-modified products (developed using 3D food printing technology) and taste-optimised products (i.e. soups, mousses, fruit and vegetable beverages, dairy desserts and seasonings) developed based on the results obtained from Stage 1 above.

Interventions

BEHAVIORALTexture-modified foods for cancer patients (Stage 2)

Participants (cancer patients that require texture-modified foods) will be expected to evaluate a maximum of three meals over a 2-weeks period.

BEHAVIORALTaste-optimised foods for cancer patients (Stage 3)

Participants (cancer patients with taste & smell alterations) will be expected to evaluate three foods at home over a period of one month.

Sponsors

AZTI Spain
CollaboratorUNKNOWN
Maspex Poland
CollaboratorUNKNOWN
Natural Machines Spain
CollaboratorUNKNOWN
University of Warsaw
CollaboratorOTHER
University of Reading
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
OTHER
Masking
SINGLE (Subject)

Masking description

All samples provided to the participant are labelled with 3 digit random codes.

Intervention model description

This is a 3 stage study design. The first stage will be a qualitative part with interviews and focus group sessions. In the second and third stages participants will evaluate food products. The second and third stages of the study will be conducted single blind as it is not feasible to blind the researcher.

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

1. Stage 1 1. Group A - Patients * Adults 18-65 years old. * Currently undergoing oncological treatment or have undergone oncological treatment in the last 12 months. * Patients that require or have required texture-modified foods and/ or experience or have experienced taste & smell alterations in the last 12 months. 2. Group B - Relatives and caregivers * Over 18 years old. * Relative or caregiver of an adult oncological patient (that require texture-modified foods and/ or experience taste & smell alterations). * Living/caring for someone that is currently undergoing or have undergone oncological treatment. * Participates actively in cooking and buying food for a household of which the person currently undergoing oncological treatment is a member. 3. Group C - Healthcare professionals * Dietitians, speech and language therapists, medical/clinical oncologists, cancer specialist nurses, and oncology social workers and counselors. * Minimum of a year's experience with oncological patients that require texture-modified foods and/or having taste & smell alterations. 2. Stage 2 * Adults 18-65 years old. * Currently undergoing oncological treatment or have undergone oncological treatment in the last 12 months and require or have required texture-modified foods in the last 12 months. * Individuals without dietary allergies or intolerances to the foods that will be tested in the study. 3. Stage 3 * Adults 18-65 years old. * Currently undergoing oncological treatment or have undergone oncological treatment in the last 12 months and are experiencing or have experienced taste & smell alterations in the last 12 months. * Individuals without dietary allergies or intolerances to the foods that will be tested in the study.

Exclusion criteria

* Individuals below 18 years old will be excluded from the study. * Individuals with dietary intolerances or allergies to the foods that will be tested in the study (Stages 2 and 3 only). * Individuals who do not have the ability or capacity to consent. * Individuals who are nil by mouth or have nasal gastric tubes of other feeding tubes inserted. * Individuals who need modified solid and liquid diets due to problems with swallowing (Stage 3 only).

Design outcomes

Primary

MeasureTime frameDescription
Acceptability of developed taste-optimised food 31 hour on Stage 3 visit day 3Acceptability of taste-optimised food 3 using a questionnaire. Participants will be asked to rate their liking of appearance, aroma, taste, texture and overall using a 9-point hedonic scale where 1 is dislike extremely and 9 is like extremely. They will also be asked to indicate their preference in comparison to usual products using a 5-point scale where 1 is I much preferred this product to my usual products and 5 is I much prefer my usual products to this one. They will be asked to indicate whether they would buy this product using a 5-point scale where 1 is definitely would buy and 5 is definitely would not buy.
Acceptability of developed texture-modified food 31 hour on Stage 2 visit day 3Acceptability of texture-modified food 3 using a questionnaire. Participants will be asked to rate their liking of appearance, aroma, taste, texture and overall using a 9-point hedonic scale where 1 is dislike extremely and 9 is like extremely. They will also be asked to indicate their preference in comparison to usual products using a 5-point scale where 1 is I much preferred this product to my usual products and 5 is I much prefer my usual products to this one. They will be asked to indicate whether they would buy this product using a 5-point scale where 1 is definitely would buy and 5 is definitely would not buy.
Acceptability of developed taste-optimised food 11 hour on Stage 3 visit day 1Acceptability of taste-optimised food 1 using a questionnaire. Participants will be asked to rate their liking of appearance, aroma, taste, texture and overall using a 9-point hedonic scale where 1 is dislike extremely and 9 is like extremely. They will also be asked to indicate their preference in comparison to usual products using a 5-point scale where 1 is I much preferred this product to my usual products and 5 is I much prefer my usual products to this one. They will be asked to indicate whether they would buy this product using a 5-point scale where 1 is definitely would buy and 5 is definitely would not buy.
Acceptability of developed taste-optimised food 21 hour on Stage 3 visit day 2Acceptability of taste-optimised food 2 using a questionnaire. Participants will be asked to rate their liking of appearance, aroma, taste, texture and overall using a 9-point hedonic scale where 1 is dislike extremely and 9 is like extremely. They will also be asked to indicate their preference in comparison to usual products using a 5-point scale where 1 is I much preferred this product to my usual products and 5 is I much prefer my usual products to this one. They will be asked to indicate whether they would buy this product using a 5-point scale where 1 is definitely would buy and 5 is definitely would not buy.
Acceptability of developed texture-modified food 11 hour on Stage 2 visit day 1Acceptability of texture-modified food 1 using a questionnaire. Participants will be asked to rate their liking of appearance, aroma, taste, texture and overall using a 9-point hedonic scale where 1 is dislike extremely and 9 is like extremely. They will also be asked to indicate their preference in comparison to usual products using a 5-point scale where 1 is I much preferred this product to my usual products and 5 is I much prefer my usual products to this one. They will be asked to indicate whether they would buy this product using a 5-point scale where 1 is definitely would buy and 5 is definitely would not buy.
Acceptability of developed texture-modified food 21 hour on Stage 2 visit day 2Acceptability of texture-modified food 2 using a questionnaire. Participants will be asked to rate their liking of appearance, aroma, taste, texture and overall using a 9-point hedonic scale where 1 is dislike extremely and 9 is like extremely. They will also be asked to indicate their preference in comparison to usual products using a 5-point scale where 1 is I much preferred this product to my usual products and 5 is I much prefer my usual products to this one. They will be asked to indicate whether they would buy this product using a 5-point scale where 1 is definitely would buy and 5 is definitely would not buy.

Secondary

MeasureTime frameDescription
Interviews1 hour session on Stage 1 visit day 1Discussion on food related issues faced by cancer patients requiring texture-modified diets / having taste & smell alterations via interviews.
Focus group2 hour session on Stage 1 visit day 2Discussion on food related issues faced by cancer patients requiring texture-modified diets / having taste & smell alterations with relatives/caregivers of cancer patients via a focus group session.
Food diary7 consecutive daysRecord of all that is eaten or drunk and any problems encountered during/after eating from cancer patients and relatives/caregivers of cancer patients.

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026