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EpilepsyMCP-EpiNCT06898749

Impact of Canine Mediation Practice in Psychomotor Therapy on Improving the Quality of Life in Adult Epileptic Patients.

A study testing canine mediation and standard psychomotor therapy in people with Epilepsy, run by Fondation Ophtalmologique Adolphe de Rothschild at 2 sites in France.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

In addition to the search for new pharmaceutical or surgical solutions that could improve the therapeutic management of epileptic individuals, it is interesting to ask whether other complementary approaches, such as canine mediation in psychomotor therapy, could enhance the quality of life in this population. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Epilepsy
What is being tested?
canine mediation and standard psychomotor therapy
Could I receive a placebo?
No, everyone receives an active treatment
How many people
76 participants
Where
2 sitesFrance
Study dates
14 Sep 2026to Mar 2030
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Person aged ≥ 18 years
  • Presenting pharmacoresistant epilepsy according to the criteria of the International League Against Epilepsy
  • Requiring psychomotor therapy sessions for one of the following indications:
  • Difficult emotional and relational management And/or global motor difficulties And/or body schema organization disorder And/or temporo-spatial disorder
  • Explicit consent or no opposition to participation in the study by the patient and/or their legal representative or guardian
  • Image rights consented by the patient and their legal representative or guardian, if applicable
  • Hospitalization or residence at the Teppe Institute or at the FAM (Foyer d'Accueil Médicalisé) des 4 Jardins planned for at least 3 months
  • Affiliated with or a beneficiary of a social security scheme

Who cannot join

  • Fear or phobia of dogs
  • Epileptic person benefiting from a legal protection measure other than guardianship or curatorship
  • Person with insufficient cognitive abilities to respond to the questionnaires
  • Pregnant or breastfeeding woman

Trial locations and contacts

2 sites in 1 country. Contact the study team or a site near you to ask about taking part.

Amelie Yavchitz contact

+33148036454

ayavchitz@for.paris

France2 sites, 2 recruiting
  • Fondation Partage et Vie - FAM Les Quatre Jardins

    Saint-Étienne-de-Saint-Geoirs, 38590

    Mathilde CHALENDARD, 0475075959, mathilde.chalendard@teppe.org

    Not yet recruiting
  • Institut La Teppe

    Tain-l'Hermitage, 26600

    Nicolas MEZOUAR, Dr, +33475075959, nicolas.mezouar@teppe.org

    Institut La Teppe

    Recruiting

Other trials in France

About this study

In addition to the search for new pharmaceutical or surgical solutions that could improve the therapeutic management of epileptic individuals, it is interesting to ask whether other complementary approaches, such as canine mediation in psychomotor therapy, could enhance the quality of life in this population.

However, there is currently no evidence indicating that exposure to animals through mediation sessions would be beneficial for epileptic individuals, particularly regarding their quality of life, anxiety, emotional management, or cognition (such as social cognition). In the absence of current data in this population, it seems pertinent to study the impact of this practice on people with epilepsy. Furthermore, beyond quality of life, it would be valuable to examine whether it also influences anxiety or the frequency of seizures in individuals with epilepsy (a phenomenon reported for epileptic individuals living with a pet dog or a service dog). Canine mediation could help better manage and regulate the emotions of epileptic individuals, as well as improve their self-esteem.

Conditions
Epilepsy
Being tested
canine mediation, standard psychomotor therapy
Medical subject headings
Epilepsy

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • canine mediationOther

    Animal mediation consists of bringing an animal into contact with a specific audience to improve the mental or physical health of a person. The dog and beneficiaries interact through various activities, in which the animal participates, offered during the sessions. The dog plays a particularly important role as a mediator through the bonds it forms with the human, as well as a non-judgmental partner in interaction.

    The canine educator will be accompanied by a healthcare professional during interventions. The sessions are organized based on the expertise and suggestions of both professions (canine educator and psychomotor therapist).

    The canine educator will be a state-certified professional educator with a specialization in animal mediation.

    The dog used is trained by the educator, with two types of learning being worked on: emotions and "commands" on cue.

  • standard psychomotor therapyOther

    standard sessions of psychomotor therapy

Study groups in NCT06898749
Study groupRoleWhat they receive
canine mediation in psychomotor therapyExperimentalGroup psychomotor therapy sessions combined with canine mediation (1 session per week for 10 weeks)
Receives: Other: canine mediation
standard psychomotor therapyActive comparatorStandard group psychomotor therapy sessions (1 session per week for 10 weeks)
Receives: Other: standard psychomotor therapy

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Improvement of quality of life

    Increase in the Quality of Life in Epilepsy Inventory-31 (QOLIE-31) score of at least 5 points between inclusion and one week after the completion of the 10 sessions.

    The score of the QOLIE-31 (Quality of Life in Epilepsy Inventory-31) ranges from 0 to 100. A score of 0 represents the worst possible quality of life, while a score of 100 represents the best possible quality of life.

    Measured: Day 0 and Day 7 after the end of the 10 sessions

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted27 Mar 2025
  2. Study start14 Sep 2026
  3. Primary completionMar 2030 (estimated)
  4. Study completionMar 2030 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Other
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
76 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06898749
Sponsor's protocol ID
NMR_2024_8
Acronym
MCP-Epi
Status last verified
Oct 2026
First submitted
21 Mar 2025
Last updated
6 Oct 2026
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing canine mediation and standard psychomotor therapy in people with Epilepsy, run by Fondation Ophtalmologique Adolphe de Rothschild at 2 sites in France.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 8 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 6 Oct 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in France. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Amelie Yavchitz (+33148036454, ayavchitz@for.paris), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Improvement of quality of life (time frame: Day 0 and Day 7 after the end of the 10 sessions). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 6 Oct 2026.

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