Investigation of the Effects of Proprioceptive Neuromuscular Facilitation Exercises in Patients With Myasthenia Gravis

Hacettepe University

Status

Completed

Conditions

Myasthenia Gravis

Treatments

Other: proprioceptive neuromuscular facilitation exercise

Study type

Interventional

Funder types

Other

Identifiers

NCT06158815

KA-22017

Details and patient eligibility

About

The goal of this clinical trial is to investigate of the effects of proprioceptive neuromuscular facilitation exercises on fatigue, muscle strength and functional parameters in patient with Myasthenia Gravis. The main questions it aims to answer are:

Do proprioceptive neuromuscular facilitation exercises reduce fatigue in patients with Myasthenia Gravis?
Do proprioceptive neuromuscular facilitation exercises increase muscle strength in patients with Myasthenia Gravis?
Do proprioceptive neuromuscular facilitation exercises improve functional parameters in patients with Myasthenia Gravis?
How well can patients with Myasthenia Gravis tolerate proprioceptive neuromuscular facilitation exercises? Participants will be divided into 2 groups as control group and exercise group with block randomization method. In this single-blind randomized controlled study, the participants in the control group will be placed on a waiting list without any intervention during the 6-week study period and at the end of the study, the interventions applied to the exercise group will be applied exactly the same. Proprioceptive neuromuscular facilitation exercises will be applied to the exercise group 3 days a week, 1 hour a day for 6 weeks. Individuals will be evaluated at the beginning and at the end of the study.

Researchers will compare exercise and control group to see if there are effects of proprioceptive neuromuscular exercises patients with Myasthenia Gravis.

Enrollment

23 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Volunteering to participate in the study
Being between the ages of 18-65
It must be confirmed by the Neurologist that the patient has been diagnosed with adult onset and Achr+ generalized Myasthenia Gravis and has been in a stable condition for the last 6 months.
Being in class II or III according to the American Myasthenia Gravis Foundation Clinical Classification

Exclusion criteria

Having a cognitive problem or having a Mini Mental Test score below 24
Change in the type and dose of medical treatment within the last 6 months
Having another cardiorespiratory, metabolic, systemic, rheumatological, orthopaedic and neurological disease (unstable and at a level that prevents participation in the exercise programme) in addition to Myasthenia Gravis
Having a body mass index below 17 kg/m2 and above 30 kg/m2
Having participated in any physiotherapy program any intervention study for the last 6 months
Having undergone pregnancy, birth or surgical operation in the last 6 months.