Feasibility Study of the Taïso Practice in Parkinson's Disease (Taïso-Park)

University Hospital, Angers

Status

Completed

Conditions

Parkinson Disease

Treatments

Other: Taïso

Study type

Interventional

Funder types

Other

Identifiers

NCT04045925

2019-A01551-56

Details and patient eligibility

About

This is a pilot study of descriptive and analytical, prospective feasibility, monocentric, longitudinal with 6 months of bi-weekly practice of Taïso in patients with Parkinson's disease with mild to moderate postural instability.

The intervention is planned over 6 months (25 consecutive weeks) for the whole project of the patient group. Patients are included in the month before the start of the treatment of the intervention. Four standardized evaluation sessions are conducted: a first evaluation during the first week of Taiso and then every 8 weeks (2 months, 4 months and 6 months). Incident collection and fitness assessment tests are performed by the physical trainer while the balance and are performed by a physiotherapist. The quality of life assessment and the MDS-UPDRS II rating are performed during the inclusion visit and then the final study visit (within 2 weeks) after 6 months of practice) with the coordinating neurologist. An evaluation of incidents is also carried out during this end-of-study visit.

Enrollment

12 patients

Sex

All

Ages

18 to 85 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Age ≥18 and <85 years old,
Parkinson's disease diagnosed by a neurologist, treated and sensitive to dopaminergic treatment without limitation of the duration of the disease since the date of diagnosis,
Patient with mild to moderate postural instability (equivalent to grade 2.5 and 3 on the Hoehn and Yahr scale),
Naive patient of any practice of Taiso,
Patient available to perform the Taïso program planned in the study,
Patient with written informed consent

Exclusion criteria

Patient with a contraindication to the practice of sport
Pregnant woman, parturient and breastfeeding mother
Patient deprived of liberty by administrative or judicial decision
Patient admitted to a health or social facility for purposes other than that of research
Adults under guardianship or trusteeship or unable to express consent
Patient not affiliated to a social security system
Patient already participating in a therapeutic research protocol that aims to improve physical or mental abilities