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Describe to Better Understand, the Mealtime of People With Parkinson's Disease Dependent on Food Intake

Describe to Better Understand, the Mealtime of People With Parkinson's Disease Dependent on Food Intake

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05898139
Acronym
AideAlimPark
Enrollment
22
Registered
2023-06-12
Start date
2024-02-01
Completion date
2025-10-13
Last updated
2025-12-22

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

Conditions

Deglutition Disorders, Parkinson Disease

Keywords

Dysphagia, Assistance feeding, Parkinson disease, Caregivers, Mealtime

Brief summary

The main objective is to describe strategies (verbal, non-verbal (gesture, intonation), and environmental), designed and used by the assisting/aided dyad to feed a dysphagic dependent person by articulating the safe and hedonic dimensions in the context of Parkinson's disease or atypical parkinsonian syndrome during a meal

Detailed description

It is described in the literature that being helped for the meal disrupts the pre-oral phase in the visual and proprioceptive afferences received by the sick person to prepare neurologically the other phases of swallowing. In cases of dysphagia, regardless of the cause, the need for food assistance is correlated with higher mortality and an increased risk of pneumonia. Thus, whether at home or in an establishment, human help is often put in place to facilitate the time of the meal, make it more effective (limitation of the duration of the meal, maximization of the nutritional amounts ingested) and safe (prevention of the occurrence of wrong driving). Our hypothesis is that representations about food and aid at meal times, as well as the attitudes of both the helper and the helped, are factors influencing the realization of an adapted human aid when eating a meal in a dependent person. An observation of a meal during a hospitalization and an interview with the sick person and his caregiver are carried out independently. Between 15 days and a month after the first visit, excerpts from the film will be presented and commented by the dyad according to the technique of self-confrontation. A report of the thematic elements identified during the interviews will be proposed for validation by the dyad. This visit can be made during a scheduled appointment in the hospital, by videoconference or at home if the participants do not have access to a videoconference system.

Interventions

None listed

Sponsors

University Hospital, Toulouse
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

For patients: Inclusion Criteria: * Patient with typical or atypical Parkinsonian syndrome, collected in the medical record * Indication of swallowing disorders or dysphagia, according to item 2.3 chewing and swallowing, part II of the MSD/UPDRS scale or collection in the medical record * Person dependent on food (according to MDS/UPDRS - food tasks item, part II, 2.4 ≥ 2, to be help to cut food punctually * Having a usual caregiver present for the meal. * Affiliated person or beneficiary of a social security scheme. * Free, informed, written and signed consent by participant and investigator (no later than the day of inclusion and prior to any review required by the research)

Exclusion criteria

* Individuals whose cognitive state does not allow simple questions to be answered, as judged by the neurologist * Person fed exclusively by enteral nutrition. * Patient who refuses to be filmed For caregivers: Inclusion Criteria: * caregiver of the patient for at least 2 months for the taking of meal * Person with French language to answer the questions of the interview

Design outcomes

Primary

MeasureTime frameDescription
Strategies description13 monthsDescription of the strategies designed and used by the assisting/aided dyad to feed dysphagic patients to perform the hand-to-mouth gesture in the context of Parkinson's disease or atypical parkinsonian syndrome during a meal, using filmed data and semi-directional interviews.

Secondary

MeasureTime frameDescription
Description of the perception of meal time, patient's point of view13 monthsThematic analysis of the perception of meal timing, diet, meal assistance for the sick person.
Description of the perception of meal time, helper's point of view13 monthsThematic analysis of the perception of meal timing, diet, meal assistance for the caregiver
Description of quality of life related to meal time13 monthsIdentify factors that contribute to and detract from meal-related quality of life satisfaction.
Identification of specific needs for educational programmes13 monthsIdentify the needs of carers to adapt or place specific educational programmes
Description of strategies put in place during meal time13 monthsOverview of the strategies put in place to promote a compromise between nutritional, safety and hedonic objectives

Countries

France

Outcome results

None listed

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