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Effect of Sensorimotor Training on Upper Extremity in Parkinson's Patients

Investigation of the Effect of Sensorimotor Training on Upper Extremity Functions, Activity and Participation in Parkinson's Patients

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05241015
Enrollment
27
Registered
2022-02-15
Start date
2021-12-08
Completion date
2023-11-20
Last updated
2024-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Parkinson Disease

Keywords

Parkinson, Upper Extremity, Sensorimotor Training, ICF, Function

Brief summary

There are many factors affecting the upper extremity such as tremor, bradykinesia, rigidity, and postural instability in Parkinson's patients. According to the International Classification of Functioning, Disability and Health (ICF) model, there are restrictions on people's activities and participation in life due to structural and functional disorders affecting the upper extremity in PD. In PD, integrating and using proprioceptive feedback, sensorimotor integration and peripheral sensory functions are reported to be impaired. Numerous studies show that the main source of motor problems in PD is dysfunction of sensorimotor integration. Since the cervical region contains a dense concentration of proprioceptive organs such as muscle spindles, it plays an important role in providing afferent proprioceptive information for postural control. Therefore, sensorimotor training targeting the cervical region gains importance. In this study, we aim to reduce PD-specific upper extremity disorders and related activity and participation limitations by increasing motor control in the cervical region with sensorimotor training. Patients with Parkinson's disease will be included in the study and randomly divided into 2 groups. While the general physiotherapy program will be applied to the control group, sensorimotor training will be given in addition to the exercise group.

Interventions

OTHERControl Group

Treatment protocol; It will be applied to improve posture, strengthen muscles, eliminate shortness, increase flexibility, balance/coordination, sit up/stand up and in-bed mobilization, and improve gait. Before taking the treatment, a general evaluation will be made and as a result of this evaluation, muscle shortness, loss of strength, postural disorders and the activities and positions they have the most difficulty in daily life will be determined. Treatment programs will be shaped according to the problems determined in line with the evaluations made.

In addition to the standard physiotherapy program, sensorimotor training including the cervical region will be given to the this group. Deep cervical flexor and extensor muscles, which provide stability in the cervical region, will be trained. A Pressure Biofeedback Device will be used to train the deep cervical flexors. Both positional and kinesthetic sensory training will be provided by maintaining the stability of the cervical region by means of the laser kit that provides visual feedback.Additionally, oculomotor exercises will be given.

Sponsors

TC Erciyes University
CollaboratorOTHER
Nuh Naci Yazgan University
CollaboratorOTHER
Hacettepe University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
40 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Having idiopathic Parkinson's disease over the age of 40 * Meets the diagnostic criteria of the United Kingdom Parkinson's Disease Society Brain Bank * Hoehn-Yahr Staging \<3 * Mini mental test score of 24 and above * In the on period * Receiving oral therapy only

Exclusion criteria

* Patients receiving device-assisted therapy * Patients receiving apomorphine therapy * Patients with mini mental test scores below 24 * Patients who use drugs (antidepressants, etc.) that will affect cognitive functions * Patients with hearing and speech problems * Patients with orthopedic, neurological and vestibular problems other than Parkinson's that may prevent them from completing the tests and treatment

Design outcomes

Primary

MeasureTime frameDescription
Posture AnalysisChange from baseline at 8 weekNew York Posture Rating Chart
TremorChange from baseline at 8 weekFahn; Tolosa, Marin Clinical Tremor Rating Scale will be used to evaluate tremor. Each item was scored between 0-4. A lower score is an indicator of better status.
Unified Parkinson's Disease Rating ScaleChange from baseline at 8 weekUnified Parkinson's Disease Rating Scale is a scale that evaluates disability and disorders related to Parkinson's and consists of 4 main subtitles and 42 questions in total . Each item was scored between 0-4 . A lower score is an indicator of better status.
ProprioceptionChange from baseline at 8 weekFor proprioception, joint position error in the cervical region and upper extremity will be evaluated with the laser kit.
Tactile acuityChange from baseline at 8 weekFor upper extremity tactile acuity, moving 2-point discrimination test (MTPD) will be performed using an esthesiometer.
Touch thresholdChange from baseline at 8 weekSemmes Weinstein Monofilament Test will be used to evaluate upper extremity touch threshold.
Pain thresholdChange from baseline at 8 weekAlgometer will be used to evaluate upper extremity pain threshold.
Pain intensityChange from baseline at 8 weekVisual pain scale (VAS) will be used to evaluate upper extremity pain.In the evaluation, pain averages ranging from 0 to 10 cm are given. 0 indicates that there is no pain, while as the score increases, the severity of pain increases.
Hand Grip StrengthChange from baseline at 8 weekHand Dynamometer will be used to measure hand grip strength.
Pinch Grip StrengthChange from baseline at 8 weekPinch meter will be used to measure pinch grip strength.
Endurance of Cervical MusclesChange from baseline at 8 weekCraniocervical Flexion (CSF) test, Evaluation of cervical flexor-extensor muscles
FatigueChange from baseline at 8 weekParkinson's Fatigue Scale will be used to evaluate fatigue. It is consists of 16 items related to presence of fatigue. All items are scored by patients using a five-point Likert-type scale including response options ranging from '(1) strongly disagree' to '(5) strongly agree'. A higher score indicates a higher level of fatigue.
Hand functionsChange from baseline at 8 weekPurdue Pegboard Test (PPT)
Dual Task PerformanceChange from baseline at 8 weekDuring the Purdue Pegboard Test, the second task will be added and the completion time will be recorded.
Disabilities of the Arm, Shoulder and Hand QuestionnaireChange from baseline at 8 weekIt will be used to determine the problems experienced in the use of the upper extremity. It consists of 3 sections. All questions are answered according to a 5-point Likert system. A score between 0-100 is obtained from each section. The higher the score, the higher the disability.
Quality of life evaluationChange from baseline at 8 weekParkinson's Disease Questionnaire (PDQ-39) will be used to evaluate quality of life. It contains 39 items in total. A score between 0 and 4 is given for each question. A high overall score indicates worsening quality of life.
Evaluation of Environmental FactorsChange from baseline at 8 weekQuestions structured by the researchers will be used on the issues of support and attitudes under the environmental factors heading of the ICF model. Questions are scored between 0 and 10. A high score indicates high satisfaction.
Motor speedChange from baseline at 8 weekMotor speed will be evaluated using the Finger tapping test.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026