Transcranial Photobiomodulation With Patients With Parkinson's Disease

NCT ID: NCT06729125

Last Updated: 2025-04-08

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

38 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-12-15

Study Completion Date

2025-04-03

Brief Summary

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Parkinson's disease (PD) is the second most common neurodegenerative disorder after Alzheimer's disease. It is a progressive and disabling disease with significative impact on quality of life. Since it has no cure, available treatment is targeted to improve the symptoms due to a lack of dopamine in the central nervous system. The aim of the study was to see how transcranial photobiomodulation (tPBM) helped patients with Parkinson's disease.

Detailed Description

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Conditions

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Parkinson Disease

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Investigators

Study Groups

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study group

Group Type EXPERIMENTAL

transcranial photobiomodulation

Intervention Type DEVICE

Single-session transcranial laser stimulation was administered with a continuous-wave, 1,064-nm laser (Model CG-5000 Laser, Cell Gen Therapeutics LLC, Dallas, TX).

control group

Group Type ACTIVE_COMPARATOR

exercises training

Intervention Type OTHER

balance exercises and others

Interventions

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transcranial photobiomodulation

Single-session transcranial laser stimulation was administered with a continuous-wave, 1,064-nm laser (Model CG-5000 Laser, Cell Gen Therapeutics LLC, Dallas, TX).

Intervention Type DEVICE

exercises training

balance exercises and others

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* idiopathic PD,
* Hoehn \& Yahr stage I-IV,
* independent gait with or without technical assistance
* stable parkinsonian medication for at least a month before the study star.

Exclusion Criteria

* comorbidities that affect balance or walking,
* other neurological pathologies besides PD,
* chronic diseases not medically controlled and participation in another physiotherapy program or sport activity during the intervention period or in the month before starting the study
Minimum Eligible Age

50 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Al-Zaytoonah University of Jordan

OTHER

Sponsor Role lead

Responsible Party

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Hanan Hosny M Battesha

associate professor hanan hosny M Battesha

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Al Zaytoonah University

Amaan, , Jordan

Site Status

Countries

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Jordan

Related Links

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Other Identifiers

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PD , LASER

Identifier Type: -

Identifier Source: org_study_id

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