Can simple insoles or special exercises restore balance in diabetic nerve damage?

NCT ID NCT07712289

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 Results may not be published yet.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
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jul 17, 2026 · Last updated Jul 17, 2026

Summary

This study tests two approaches to help people with diabetic neuropathy improve their balance. One group uses textured insoles in their shoes, while the other group does a series of quick stretches and compressions called Rood's facilitatory technique. Both groups also receive contrast baths. The trial lasts four weeks and measures balance and nerve function.

What this could mean

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

Active substance
textured insoles and Rood's facilitatory technique (quick stretch and heavy compression)
What this could lead to
If successful, this could point toward simple, low-cost ways to improve balance and reduce fall risk in people with diabetic neuropathy.
What could go wrong
This is a small, early-stage trial with only 44 participants, so results may not apply to everyone. The improvements might be modest or not last long-term.

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

44 people

The number who actually took part.

Started

Mar 2025

Finished

May 2025

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

45 to 60 years

Sex

Anyone

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 * Participants must have a clinical diagnosis of Type 2 diabetes. * Participants must show evidence of diabetic peripheral neuropathy (DPN) as diagnosed by clinical examination. * Participants with 25-40 Berg Balance Score. * Participants with 6-8(Patient version) and 2.5-4(Physical assessment) Michigan Neuropathy Score. * Participants aged 45 years to 60. * Participants taking medications. * Participants must be able to understand the study procedures and provide written informed consent. Exclusion Criteria * Participants who have significant cognitive impairments (e.g., dementia) that would prevent them from understanding and adhering to study instructions. * Participants with severe PAD or significant circulatory problems that would contraindicate the use of insoles or tactile stimulation therapy. * Participants with other neurological conditions that could confound the results. * Participants who have had recent surgery or trauma to the feet or lower extremities in the past 6 months. * Participants who are involved in another clinical trial. * Participants with active diabetic foot ulcers, severe deformities, infections, or other complications that would make it unsafe or inappropriate to use textured insoles.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

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

Contacts and locations

Locations

  • The University of Faisalabad

    Faisalābad, Punjab Province, 38000, Pakistan

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