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Therapeutic Education in Parkinson's Disease: What Impact on Drug Representations of Patients? (ETPARK-REMED)

Therapeutic Education in Parkinson's Disease: What Impact on Drug Representations of Patients?

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04228523
Acronym
ETPARK-REMED
Enrollment
24
Registered
2020-01-14
Start date
2020-02-24
Completion date
2021-01-01
Last updated
2026-05-06

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

Conditions

Parkinson Disease

Keywords

Therapeutic education, Parkinson Disease, Socials representations

Brief summary

Dopaminergic drug can have adverse effects leading to potential serious consequences. Therapeutic patient education must promote the understanding of drugs to improve its management. This study tries to evaluate the effect of therapeutic education workshop on Parkinson disease's drug (drug workshop) on the evolution of drug's representations in patients with Parkinson's disease compared to a control group.

Detailed description

Dopaminergic drug can have adverse effects leading to potential serious consequences. Therapeutic patient education must promote the understanding of drugs to improve its management. The therapeutic educational program ETPARK includes individual's consults or workshop. The team frequently offer to patients to participate in workshop on Parkinson disease's drug. This study tries to evaluate the effect of therapeutic education workshop on Parkinson disease's drug (drug workshop) on the evolution of drug's representations in patients with Parkinson's disease compared to a control group (speaking group) at 1 and 3 months.

Interventions

OTHERTherapeutic education workshop

Workshop on Parkinson disease drug has several educative sequences (lasting 4hours). * A first round table is organized to know the needs and issues related to drug management of patients. * The 1st educative sequence consists in knowing the different class of dopaminergic drugs and their action. * The 2nd educative sequence leads patients to understand their prescription and be aware of the needs to take pills regularly. * The 3rd educative sequence consists in learning and identifying potentials adverse effects and finds effective strategies to prevent them. At the end, one patient explains its tips and tricks about its drug management

OTHERSpeaking Therapy

Speaking group is leaded by a psychologist from Centre Expert Parkinson (lasting 2 hours). This specific time is an exchange between patients with Parkinson disease who feel free to come. It is about sharing its own experience. It is a very special moment, confidential and kindly where patients don't judge themselves and speak only if they want to.

Sponsors

University Hospital, Toulouse
Lead SponsorOTHER
France Parkinson Association
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Intervention model description

therapeutic education or speaking group

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Patients with Parkinson's disease according to the United Kingdom Parkinson Disease Society Brain Bank (UKPDSBB) criteria, * Patients who are already in therapeutic education program ETPARK, * Patients who need and want to participate in therapeutic education workshop on Parkinson disease drug, * Patients with health insurance, * Patients who have signed a written informed consent form.

Exclusion criteria

* Patients suffering from another parkinsonian syndrome (multiple system atrophy, progressive supranuclear palsy etc.), * Patients who has already done workshop on Parkinson disease drug (program ETPARK) * Patients already included in clinical trial during the study, * Patients who have severe psychiatric disorders or dopaminergic psychosis, * Patients with cognitive impairment, * Patients unable to complete the various scales used in the study, * Patients under juridical protection, * Women pregnant or breastfeeding.

Design outcomes

Primary

MeasureTime frameDescription
Evolution of Drug representation in Patients : BMQThree monthsEvolution of Drug representation through the Believe about Medicines Questionnaire (BMQ) compared to the control group. Evolution will be compared between the Baseline and the end of the study BMQ with eighteen items coded from 1 " "strongly agree" to 5 "strongly disagree".
Evolution of Drug representation in Patients : Verbal associationThree monthsEvolution of Drug representation through verbal association tasks compared to the control group. Evolution will be compared between the Baseline and the end of the study

Secondary

MeasureTime frameDescription
Drug representation in caregivers : Verbal associationDay 1Drug representation through verbal association tasks.
Drug representation in caregivers : BMQDay 1Drug representation through the Believe about Medicines Questionnaire (BMQ). BMQ with eighteen items coded from 1 " "strongly agree" to 5 "strongly disagree".
Knowledge about the diseasethree monthsEvolution between Baseline and three months with a test created for the study. The test have 8 questions with two answers possible : True or False
Evolution in life quality : VASthree monthsEvolution in life quality evaluate with Visual Analog Scale (VAS), 0 being the worst quality of life and 10 the best quality of life he can have. Evolution between Baseline and three months
Evolution in life quality : PDQ-(39)three monthsEvolution in life quality evaluate with Parkinson Disease Quotation (PDQ)-39 with thirty-nine items coded from 1 " "always" to 5 "never". The Parkinson's Disease Questionnaire (PDQ-39) assesses how often people affected by Parkinson's experience difficulties across 8 dimensions of daily living including relationships, social situations and communication. Evolution between Baseline and three months

Countries

France

Contacts

PRINCIPAL_INVESTIGATORChristine Brefel-Courbon, MD

Univeristy Hospital Toulouse

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 7, 2026