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Effect of Physical Rehabilitation in Patients With Parkinson's Disease

F

Faculty of Medicine, Sousse

Status

Not yet enrolling

Conditions

Parkinson Disease

Treatments

Other: rehabilitation

Study type

Interventional

Funder types

Other

Identifiers

NCT06021834
Faculté de Médecine de Sousse

Details and patient eligibility

About

This is a prospective study. The aim of this study is to investigate the effect of exercise retraining on cardiorespiratory parameters, postural balance, sociopsychological variables, and cognitive function in subjects with Parkinson's disease.

There will be two measurement sessions, one pre-intervention and one post-intervention (measuring cardiorespiratory parameters, evaluating dynamic and static postural balance, and assessing cognitive function).

Full description

this is a 12-week prospective study with the theme that I wish to develop in this context entitled "the effect of exercise retraining on cardiorespiratory parameters, postural balance, sociopsychological variables, and cognitive function in subjects with Parkinson's disease".

There will be two measurement sessions, one pre-intervention and one post-intervention (measuring cardiorespiratory parameters, evaluating dynamic and static postural balance, and assessing cognitive function).

The recruited subjects will be randomly assigned to two groups: a control group and an experimental group. The subjects will be invited to attend the program three times per week.

The control group will engage in an endurance training program, while the experimental group will participate in a combined endurance training and cognitive training program

Enrollment

40 estimated patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Diagnosed with Parkinson's disease according to the Movement Disorder Society (MDS) 2015 criteria.
  • Mild to moderate stage according to the Hoehn and Yahr scale.
  • No hearing or visual impairments that could hinder the integration and implementation of the rehabilitation protocol.
  • Has the ability to communicate and walk.
  • Patient has been stable on treatment for 3 months.

Exclusion criteria

  • A contraindication to engaging in cardiovascular physical activity
  • A Montreal Cognitive Assessment score (MoCA ) of less than 24.
  • A current psychiatric disorder that could make it difficult or dangerous to adhere to the research protocol.
  • Musculoskeletal impairments or excessive pain in any joint that could limit participation in an exercise program.
  • Treatment with sedative medications

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

40 participants in 2 patient groups

control group
Active Comparator group
Description:
The control group will be invited to attend the program three times per week and will engage in an endurance training program
Treatment:
Other: rehabilitation
experimental group
Experimental group
Description:
the experimental group will be invited to attend the program three times per week and will participate in a combined endurance training and cognitive training program.
Treatment:
Other: rehabilitation

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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