NCT07495462

Brief Summary

Parkinson's Disease (PD) is a progressive brain disorder that affects movement and balance. It can cause slowed movements, stiffness, tremor, balance problems, and an increased risk of falling. Many individuals with PD develop fear of movement, also referred to as kinesiophobia, and fear of falling. This condition may lead to avoidance of physical activity, which can further worsen balance and movement abilities. This study aims to determine whether adding Motor Imagery (MI) to a standard rehabilitation program can improve balance and reduce fear of movement in individuals with PD. MI is a mental practice technique in which an individual rehearses movements cognitively without actual physical execution. For example, a person may imagine standing up, walking, or climbing stairs. Although the movement is not physically performed, the brain regions involved in movement are activated. MI is safe, does not require special equipment, and may help improve motor control. Eligible participants will be randomly assigned to one of two groups. One group will receive standard physical therapy and rehabilitation exercises, while the other group will receive the same therapy combined with additional MI training. The rehabilitation program will last six weeks. The study will primarily evaluate whether this combined approach improves balance and reduces fear of movement. In addition, the potential effects of the intervention on fall risk, functional mobility and performance, fear of falling, activities of daily living, and motor function will also be examined. Assessments will be performed at the beginning of the study, at the end of treatment, and again at 12 weeks. Researchers hope to determine whether combining MI with conventional rehabilitation provides greater benefits than conventional rehabilitation alone and may help improve rehabilitation strategies for people living with PD.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
42

participants targeted

Target at P25-P50 for not_applicable

Timeline
1mo left

Started Jan 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress79%
Jan 2026Jun 2026

Study Start

First participant enrolled

January 2, 2026

Completed
3 months until next milestone

First Submitted

Initial submission to the registry

March 21, 2026

Completed
6 days until next milestone

First Posted

Study publicly available on registry

March 27, 2026

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 25, 2026

Expected
5 days until next milestone

Study Completion

Last participant's last visit for all outcomes

June 30, 2026

Last Updated

April 2, 2026

Status Verified

March 1, 2026

Enrollment Period

6 months

First QC Date

March 21, 2026

Last Update Submit

March 29, 2026

Conditions

Keywords

RehabilitationKinesiophobiaBalanceMotor Imagery (MI)

Outcome Measures

Primary Outcomes (2)

  • Change from baseline in kinesiophobia

    Kinesiophobia will be assessed using the Tampa Scale for Kinesiophobia (TSK-17). The TSK-17 is a self-reported questionnaire used to evaluate fear of movement or re-injury. Higher scores indicate greater levels of kinesiophobia.

    Baseline, at 6 weeks (end of intervention), and at 12 weeks follow-up

  • Change from baseline in balance performance

    Balance performance will be assessed using the Berg Balance Scale (BBS). The BBS is a widely used clinical scale consisting of 14 functional tasks that evaluate static and dynamic balance abilities. Higher scores indicate better balance performance.

    Baseline, at 6 weeks (end of intervention), and at 12 weeks follow-up

Secondary Outcomes (2)

  • Change from baseline in motor function

    Baseline, at 6 weeks (end of intervention), and at 12 weeks follow-up

  • Change from baseline in fall risk and functional mobility

    Baseline, at 6 weeks (end of intervention), and at 12 weeks follow-up

Study Arms (2)

Conventional Rehabilitation Group

ACTIVE COMPARATOR

Participants will receive a structured conventional rehabilitation program including balance training, gait training, strengthening exercises, and functional mobility exercises

Behavioral: Conventional Rehabilitation

Motor Imagery + Conventional Rehabilitation Group

EXPERIMENTAL

Participants will receive traditional rehabilitation along with motor imagery training.

Behavioral: Conventional RehabilitationBehavioral: Motor Imagery Training

Interventions

A structured physiotherapy program focusing on balance, gait, strength, and functional mobility training

Also known as: Control
Conventional Rehabilitation GroupMotor Imagery + Conventional Rehabilitation Group

A structured motor imagery program including guided visual and kinesthetic mental rehearsal of functional movements, applied in addition to conventional rehabilitation.

Motor Imagery + Conventional Rehabilitation Group

Eligibility Criteria

Age40 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Diagnosis of Parkinson's Disease (PD)
  • Age 40 years or older
  • Hoehn and Yahr stage between 1 and 3
  • Mini-Mental State Examination (MMSE) score of 22 or higher

You may not qualify if:

  • Presence of an additional neurological disorder
  • Movement impairment or nerve damage due to orthopedic pathology
  • Cardiopulmonary conditions that contraindicate exercise participation
  • Presence of severe dyskinesia
  • Visual or vestibular impairments that may affect balance
  • Presence of motor fluctuations (on-off periods)
  • Deep brain stimulation for Parkinson's Disease

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Sehit Prof. Dr. Ilhan Varank Sancaktepe Training and Research Hospital

Istanbul, Istanbul, 34785, Turkey (Türkiye)

RECRUITING

MeSH Terms

Conditions

Parkinson DiseaseKinesiophobia

Condition Hierarchy (Ancestors)

Parkinsonian DisordersBasal Ganglia DiseasesBrain DiseasesCentral Nervous System DiseasesNervous System DiseasesMovement DisordersSynucleinopathiesNeurodegenerative DiseasesPhobic DisordersAnxiety DisordersMental Disorders

Central Study Contacts

Büşranur Kurtça Güdük, MD

CONTACT

Pelin Yıldırım, MD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: Participants will be randomly assigned to two parallel groups receiving either conventional rehabilitation alone or conventional rehabilitation combined with motor imagery training.
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

March 21, 2026

First Posted

March 27, 2026

Study Start

January 2, 2026

Primary Completion (Estimated)

June 25, 2026

Study Completion (Estimated)

June 30, 2026

Last Updated

April 2, 2026

Record last verified: 2026-03

Data Sharing

IPD Sharing
Will not share

Locations