Can Acute Photobiomodulation Improve Balance and Cognition in Individuals With Ataxia: a Pilot Feasibility Placebo Randomized Controlled Trial.

NCT ID: NCT07296068

Last Updated: 2025-12-22

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

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

20 participants

Study Classification

INTERVENTIONAL

Study Start Date

2026-06-01

Study Completion Date

2027-12-10

Brief Summary

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Cerebellar ataxias cause progressive impairments in balance, gait coordination, motor timing, and cognitive functions such as attention and executive control (Buckner, 2013; Salmi et al., 2010; Timmann \& Daum, 2007). These symptoms substantially reduce independence and quality of life, and current treatments remain limited. There is an urgent need for safe, low-burden interventions that can support everyday functioning and potentially enhance compensatory neural processes.

Transcranial photobiomodulation (tPBM) uses red and near-infrared light (600-1100 nm) to modulate mitochondrial cytochrome-c oxidase, increasing ATP production, reducing oxidative stress, and improving cerebral blood flow (Hamblin, 2016; Salehpour et al., 2019). Several studies show that tPBM can acutely improve cognitive performance and motor control in both healthy adults and clinical groups (Barrett \& Gonzalez-Lima, 2013; Chan et al., 2019; Henderson \& Morries, 2017). A growing neurobiological literature suggests that light can penetrate posterior cortical areas sufficiently to modulate networks involving cerebellar-cortical loops (Jagdeo et al., 2012).

Importantly for ataxia, preliminary work shows that tPBM may acutely improve balance stability and gait metrics in older adults and patients with neurological conditions (Moro et al., 2022; Shin et al., 2021). In our own laboratory, we have observed immediate improvements in sway range and cognitive control in older adults after a 24-minute tPBM session applied over midline and posterior scalp regions. These medium to large size effects are consistent with enhanced sensorimotor integration and improved control of attention in distracting environments.

Given that individuals with cerebellar ataxia experience both motor incoordination and difficulties in maintaining cognitive stability under distracting conditions, tPBM is a promising non-pharmacological intervention worth preliminary investigation.

Detailed Description

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Conditions

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Ataxia

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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Sham Comparator: Sham photobiomodulation

Sham photobiomodulation. The sham device will follow the same protocol but without active light emission.

Group Type PLACEBO_COMPARATOR

Sham photobiomodulation

Intervention Type OTHER

The sham device will follow the same protocol but without active light emission.

Photobiomodulation

Acute photobiomodulation Twenty-four-minute photobiomodulation stimulation (twelve minutes at 670 nm followed by twelve minutes at 810 nm).

Group Type EXPERIMENTAL

Photobiomodulation

Intervention Type DEVICE

Photobiomodulation

Interventions

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Photobiomodulation

Photobiomodulation

Intervention Type DEVICE

Sham photobiomodulation

The sham device will follow the same protocol but without active light emission.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Age 18-70 years (inclusive)
* Diagnosis of ataxia
* Able to walk independently for at least 5 minutes, with or without an assistive device
* Able to stand safely for balance testing, with or without an assistive device
* Hemodynamically stable (stable blood pressure and heart rate at rest)
* On a stable medication regimen for ≥4 weeks prior to enrolment
* Sufficient vision and hearing (with usual aids if required) to complete balance and cognitive assessments
* Able to complete study questionnaires and cognitive tasks (with assistance for reading/writing if required)
* Able and willing to provide written informed consent

Exclusion Criteria

* Current or past history of head injury
* Use of medications acting on the central nervous system
* Active skin conditions on the forehead or scalp
* Any other major neurological disorder that could independently affect balance or cognition
* Ongoing brain stimulation therapy
* History of migraines
* Sensitive skin, allergies
Minimum Eligible Age

18 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University of Central Lancashire

OTHER

Sponsor Role lead

Responsible Party

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Jonathan Sinclair

Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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University of Central Lancashire

Preston, Lancashire, United Kingdom

Site Status

Countries

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United Kingdom

Central Contacts

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Jonathan J Sinclair, DSc

Role: CONTACT

Phone: +44787565153

Email: [email protected]

Facility Contacts

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Sinclair

Role: primary

Other Identifiers

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PMB Ataxia pilot feasibility s

Identifier Type: -

Identifier Source: org_study_id