Using Equine Therapy in Dementia Cognitive Stimulation
ETMW_DEM
Exploring Neurocognitive Stimulation in Dementia Through Equine-Assisted Therapy: A RCT Pilot Study
1 other identifier
interventional
36
1 country
1
Brief Summary
The goal of this clinical trial is to learn if integrating equine therapy in memory workshops in mild to moderate Dementias can improve cognitive function, quality of life and mood. The main question\[s\] it aims to answer is: Does the mediation of a horse in memory workshops increase its effects ? Researchers will compare traditional memory workshops, memory workshops using equine therapy and a control group to see if the equine therapy mediation will increase cognitive functions, mood and quality of life in individuals with mild to moderate Dementias. Participants will participate in 8 weekly sessions of equine therapy memory workshops / traditional memory workshops / a control group will not have any interventions during that period. All subjects will be evaluated pre and post intervention period.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Jun 2024
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
June 3, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 30, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
August 30, 2024
CompletedFirst Submitted
Initial submission to the registry
October 26, 2024
CompletedFirst Posted
Study publicly available on registry
October 29, 2024
CompletedMarch 18, 2026
March 1, 2026
3 months
October 26, 2024
March 16, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Change in Cognitive Function as Assessed by the Montreal Cognitive Assessment (MoCA)
Pre and post-intervention period, the Montreal Cognitive Assessment was used to assess cognitive function. Score range: 0 to 30; higher scores indicate better cognitive function
Baseline and ten weeks after
Secondary Outcomes (2)
Change in Depression Symptoms as Assessed by the Geriatric Depression Scale (GDS-15)
Baseline and ten weeks after
Change in Quality of Life as Assessed by the Quality of Life in Alzheimer's Disease (QoL-AD NH)
Baseline and ten weeks after
Study Arms (3)
Control group
NO INTERVENTIONTraditional memory workshop
ACTIVE COMPARATORNeurocognitive stimulation as usual
Equine assisted therapy memory workshop
EXPERIMENTALNeurocognitive stimulation mediated with a horse based on a defined protocol.
Interventions
The participants received 8 weekly sessions of 60 minutes of neurocognitive stimulation, based on French memory workshops.
The participants received 8 weekly sessions of 60 minutes, based on traditional memory workshops (French type of neurocognitive stimulation) with the mediation of a horse (example : working on associative memory by selecting which object is used for the horse between 2 presented objects).
Eligibility Criteria
You may qualify if:
- Have been medically diagnosed with Major Neurocognitive Disorders
- Scores between 0.5 and 2 on the Cognitive Dementia Rating scale (CDR) (Berg, 1982)
- Adults of all genders, aged 65 and over; and
- Willingness to participate in a memory workshop; e) willingness to interact with a horse.
You may not qualify if:
- Expressed fear, aversion, or has had a negative experience with horses
- Allergy or other medical condition which did not allow contact with horses.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
CAJOU
Le Boulou, 66160, France
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- OTHER
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Clinical neuropsychologist
Study Record Dates
First Submitted
October 26, 2024
First Posted
October 29, 2024
Study Start
June 3, 2024
Primary Completion
August 30, 2024
Study Completion
August 30, 2024
Last Updated
March 18, 2026
Record last verified: 2026-03
Data Sharing
- IPD Sharing
- Will not share