Dogs and rabbits may help dementia patients regain movement — a trial puts it to the test
NCT ID NCT07730983
First seen Jul 28, 2026 · Last updated Jul 29, 2026 · Updated 1 time
Summary
This randomized trial tests whether adding animal-assisted therapy (AAT) — structured sessions with a trained dog and/or rabbits — to standard rehabilitation can improve motor abilities, independence, and quality of life in older adults with dementia who are hospitalized in a medical rehabilitation unit. Participants will attend eight one-hour sessions over four weeks, with one group receiving standard rehab plus AAT and the other receiving standard rehab alone. The study measures changes in movement, daily living skills, fall risk, and well-being at the end of the program.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Animal-assisted therapy (AAT) with a trained dog and/or rabbits, combined with standard rehabilitation
- What this could lead to
- If it works, this could point toward a simple, enjoyable way to boost motor recovery and daily independence for people with dementia during rehabilitation.
- What could go wrong
- This is a small, early-stage trial with only 32 participants, so results may not apply widely. The therapy requires trained animals and staff, which may limit availability.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 32 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Dec 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Hospitalized in the geriatric medical and rehabilitation ward (SMR) of Institut Médical de Sologne (IMDS) * Diagnosed dementia or confirmed cognitive decline, shown by a score between 15 and 24 on the Mini-Mental State Examination (MMSE - a short standardized test of memory and thinking) * Has active motor rehabilitation goals (identified need to improve movement abilities during hospitalization) * Participant and/or their legal guardian, trusted person (personne de confiance), curator, or family member has provided written consent to participate in the study * Affiliated to a French social security scheme Exclusion Criteria: * Known allergy to the animals used in the animal-assisted therapy sessions (dog, rabbits) * Fear of animals * History of aggressive behavior toward animals * Concomitant psychiatric disorders * Needs only a stimulation and/or skills maintenance approach (no active motor rehabilitation goals) * Currently enrolled in another interventional research study (Note: A participant who was previously enrolled in another interventional study may join RÉMÉDI-A once their participation in the prior study has ended, without a washout period, provided all eligibility criteria are met.)
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Institut Médical de Sologne LNA Santé
Lamotte-Beuvron, 41600, France
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