The Effects of Ballet-Based Exercise Training on Respiratory Functions, Balance, Cognitive Functions, Peripheral Muscle Strength, Functional Capacity and Quality of Life in Patients With Parkinson's Disease

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorBezmialem Vakif University

About this trial

This study investigates the impact of an 8-week ballet-based dance therapy on people with Parkinson's disease. It aims to assess the effect of ballet on motor and non-motor symptoms, such as balance, cognitive function, functional capacity, and quality of life. The study will provide insights into the potential of ballet therapy as an effective, non-pharmacological treatment for Parkinson's disease.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age 18 years or older.

Diagnosed with Parkinson's disease.

Modified Hoehn and Yahr stages I to III.

Willingness to participate and provide informed consent.

Disqualifiers

Joint deformities or severe movement limitations that prevent participation in dance exercises.

Mental retardation (severe cognitive impairment).

Major surgery within the past 6 months.

Presence of uncontrolled cardiovascular, pulmonary, or oncological diseases.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Ballet-Based Dance Therapy

    Behavioral

    An 8-week ballet-based dance therapy program designed to improve balance, flexibility, peripheral muscle strength, cognitive functions, and overall functional capacity in Parkinson's disease patients. The therapy will be conducted twice a week, with each session lasting approximately 60 minutes. The exercises will be adapted to the participants' physical abilities and will focus on enhancing motor coordination, strength, and stability through ballet-inspired movements.

  • Standard Care with Exercise Counseling

    Other intervention

    Participants in the control group will receive standard care for Parkinson's disease, including pharmacological management and routine clinical follow-up. Additionally, they will receive a one-time exercise counseling session and an informational brochure outlining general home-based exercises appropriate for individuals with Parkinson's disease. No supervised or structured exercise sessions will be conducted.

Treatment groups

24 Participants
are divided into 2 treatment groups
Group A: Ballet-Based Dance TherapyExperimental treatment 1 intervention
Group B: Standard Care with Exercise CounselingActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Functional Capacity

Functional capacity will be assessed using the Six-Minute Walk Test (6MWT) according to American Thoracic Society (ATS) guidelines. The total distance walked will be recorded.

Time frame
At baseline and at week 9 (after 8 weeks of intervention)
2

Forced Expiratory Volume in 1 Second (FEV₁)

FEV₁ will be assessed using spirometry and reported in liters (L). FEV1 will be measured according to the guidelines of the American Thoracic Society (ATS) and the European Respiratory Society (ERS).

Time frame
At baseline and at week 9 (after 8 weeks of intervention)
3

Forced Vital Capacity (FVC)

FVC will be assessed using spirometry and reported in liters (L). FVC will be measured according to the guidelines of the American Thoracic Society (ATS) and the European Respiratory Society (ERS).

Time frame
At baseline and at week 9 (after 8 weeks of intervention)
4

Tiffeneau Index (FEV₁/FVC Ratio)

The ratio of FEV₁ to FVC will be calculated using spirometry and reported as a percentage (%).

Time frame
At baseline and at week 9 (after 8 weeks of intervention)

Secondary outcomes

1

Respiratory Muscle Strength

Respiratory muscle strength will be assessed by measuring maximal inspiratory pressure (MIP) and maximal expiratory pressure (MEP) using a digital mouth pressure device, in accordance with established respiratory assessment guidelines.

Time frame
At baseline and at week 9 (after 8 weeks of intervention)
2

Balance

Balance performance will be assessed using the Biodex Balance System. Stability indices will be calculated to evaluate postural control and balance.

Time frame
At baseline and at week 9 (after 8 weeks of intervention)
3

Cognitive Function

Cognitive function will be assessed using the Montreal Cognitive Assessment (MoCA). The MoCA is a 30-point scale ranging from 0 to 30, where higher scores indicate better cognitive performance.

Time frame
At baseline and at week 9 (after 8 weeks of intervention)
4

Peripheral Muscle Strength

Peripheral muscle strength will be assessed using a hand-held dynamometer for major lower extremity muscle groups.

Time frame
At baseline and at week 9 (after 8 weeks of intervention)

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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