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Education in Therapy of Parkinson's Disease

Not Applicable
Completed
Conditions
Parkinson Disease
Interventions
Behavioral: therapeutic education program
Registration Number
NCT01717144
Lead Sponsor
University Hospital, Toulouse
Brief Summary

Parkinson's disease (PD) has considerable impact on motor, psychological and social activities and significantly affects the quality of life of patients and their families. To improve the medical care of PD patients, the investigator have developed an educational program specific to PD.

The principal aim of this study is to evaluate the therapeutic education Program, comparing the quality of life of PD patients with or without the educational program after six month and one year follow-up.

The secondary aims are to evaluate the evolution of motor and psychological states in these 2 groups of patients and to compare the medical costs.

This is a monocentric, comparative, prospective randomised study. The investigators will evaluate 120 PD patients, 60 patients benefiting of the educational program and 60 patients with a traditional medical care. Quality of life of PD patients is evaluated using a specific scale (PDQ39) and a generalist scale (SF36) at 6 and 12 months. Motor and psychological states were assessed with UPDRS and HAD Scales. The educational program consisted of both individual and collective educational consultations.

The investigators supposed that the therapeutic education program will improve the quality of life of PD patients. The supposition that this improvement will correlate with the motor and psychological states.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
120
Inclusion Criteria
  • Patients with clinical diagnosis of Parkinson's disease according to the criteria of the UKPDSBB
  • Parkinson's disease patients with a score ≤4 on the Hoehn and Year scale
  • Patient without cognitive disorders
  • Patients treated with dopaminergic antiparkisonian drugs (L-DOPA, dopamine agonists,ICOMT...) or DBS stimulation (since at least 3 month)
  • Patients able to fulfil self-administered questionnaire
  • Patients affiliated to a social protection program
Exclusion Criteria
    • Patients suffering from an other pathology causing chronic pain (rheumatic disease, traumatic or orthopaedic pathologies...)
  • Parkinson's disease patients with a score>5 on the Hoehn and Yahr scale
  • Patients suffering of parkinsonism induce by drugs
  • Patients with important tremors during a OFF conditions
  • Patients ever included in another study
  • Patients with severe psychiatric disease
  • Patients under tutelage, curatelle or law protection
  • Patients included in an other clinical study
  • Patients unable to fulfil scales of the study

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
therapeutic education programtherapeutic education programThe educational program consisted of both individual and collective educational consultations with a therapeutic education nurse
Primary Outcome Measures
NameTimeMethod
Quality of life with the PDQ39 scale1 year
Secondary Outcome Measures
NameTimeMethod
Quality of life with the SF36 scale1 year
the motor state with UPDRS (Unified Pakinson's disease Rating Scale)1 year
Evaluation of social adaptation with SAS-SR (Social adjustement Scale Sel-Report) scale1 year
The psychological state with HAD (Hospital Anxiety and Depression) scale1 year
Evaluation of medical costsover the 12 months follow-up

Trial Locations

Locations (1)

UH Toulouse

🇫🇷

Toulouse, France

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