Light-Pod training may boost neck pain recovery

NCT ID NCT07005076

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
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Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jul 08, 2026 · Last updated Jul 09, 2026 · Updated 1 time

Summary

This study tests whether adding technology-assisted exercises—using light pods to improve reaction time and movement—to standard physiotherapy helps women with chronic neck pain more than exercise alone. Participants will have their pain, balance, and walking ability measured before and after the program. The goal is to see if tech-enhanced training leads to better daily function and pain relief.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
technology-assisted exercise program (reaction time light pods and exercise set)
What this could lead to
If it works, this could show that adding simple tech tools to standard exercises helps people with chronic neck pain recover faster and move better.
What could go wrong
This is a small, early-stage study with only 42 women in one city, so results may not apply to everyone. The technology may not provide extra benefit over conventional exercises alone.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

42 people

The number who actually took part.

Started

Aug 2024

Finished

Mar 2026

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 to 59 years

Sex

Female participants only

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Non-specific neck pain diagnosis * Having neck pain persisting for at least 3 months * Having the ability to speak and comprehend Turkish fluently * A pain score of 3 or higher according to the Numerical Rating Scale * A score of 5 or higher on the Neck Disability Index Exclusion Criteria: * Having a history of spinal surgery. * Having an additional musculoskeletal disorder affecting the cervical region and upper extremities (e.g., scoliosis, rheumatoid arthritis, fibromyalgia, etc.). * Receiving physical therapy and/or other treatments for any reason within the last 6 months. * Having a diagnosed psychiatric disorder. * Having a vestibular pathology. * Having visual problems despite using visual aids. * Being pregnant. * Having a neurological deficit that may affect balance. * Discontinuing or being unable to complete the treatment process.

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As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Afyonkarahisar Health Sciences University

    Merkez, Afyonkarahisar, 03030, Turkey (Türkiye)

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