ClinicalTrials.gg
Enrolling by invitationNCT06904417FeMUpdated Apr 1, 2025

Effect of Feldenkrais Method in Enhancing Postural Control for Patients with Diabetic Polyneuropathy

A Phase 1 interventional study of The Feldenkrais-based intervention and conventional balance training program in Diabetic Polyneuropathy, sponsored by Cairo University. Enrolling by invitation at 1 site in Egypt. Open to participants aged 45 Years to 60 Years. Per ClinicalTrials.gov, last updated 2025-04-01.

Sponsored by Cairo University · Phase 1, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Apr 2025, 1 year 6 months ago, but the record still lists the study as enrolling by invitation.
Phase
Phase 1
Study type
Interventional
Enrollment
24
Allocation
Randomized
Ages
45 Years to 60 Years
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-13

Among 31 studies in Diabetic Neuropathies with a site in Egypt — 9 open to participants now, 9 under way, none of them phase 3. Diabetic Neuropathies · Egypt.

Planned enrollment
21st of 22
24 · median 60
Started
2025
with 4 others
Phase 1
Only one
of the 31
Registered
24th of 31
by date
Lead sponsor
7 of 31
Cairo University

Among the 31 studies in Diabetic Neuropathies with a site in Egypt, this one is the 21st largest by planned enrollment of the 22 interventional ones that give a count, is one of 5 that started in 2025, is the only one in phase 1, and was the 24th registered.

Diabetic Neuropathies

538 studies on the registry are indexed under Diabetic Neuropathies; 80 are open to participants now.

Browse Diabetic Neuropathies studies →

Open to participants now

9 of the 31 studies in Diabetic Neuropathies with a site in Egypt are open now. Recruiting first, the newest first:

3 more — sign in →

All 9 open studies →

A study can be open while its sites in Egypt have not opened yet or have stopped. Only those recruiting at a site in Egypt →

Who these studies take

Of the 52 Diabetic Neuropathies studies recruiting now, 21 (40%) set no upper age limit and 24 (46%) stop at 75 or younger; 6 take children under 18; 3 take healthy volunteers.

This study: 45 Years to 60 Years · all sexes · no healthy volunteers.

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Watch this landscapeDownload CSVNarrow it in search →With an account: a weekly mail of what changed among 31 studies in Diabetic Neuropathies with a site in Egypt, or all of them as a file.
02

Study summary

Background: Postural Control is a major complication of polyneuropathy, affecting patients suffering from diabetes mellitus. Purpose: To examine the effect of the Feldenkrais Method on dynamic balance, limits of stability and fear of falling in adults aged 45 to 60 years with diabetic polyneuropathy in the short and mid-term. Methods: A single-blinded, parallel, multicentric randomized control trial was conducted in two health centers. Adults aged 45 to 60 years with diabetic polyneuropathy and a history of falls or dynamic balance dysfunction were recruited from hospital databases and randomly assigned to either the study or control group. The study group received 16 sessions of Feldenkrais-based sensorimotor training. Both groups received diabetic foot care instructions and traditional balance exercises. Outcomes were measured at 3 and 6-month follow-up intervals. Dynamic balance was assessed using the Timed Up and Go (TUG) Test, limits of stability using Biodex and fear of falling with the Falls Efficacy Scale (FES).

03

Conditions studied

  • Diabetic Polyneuropathy

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Keywords

  • Feldenkrais Method
  • Postural Control
  • Diabetic Polyneuropathy
04

Who can participate

Ages eligible
45 Years to 60 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Individuals must have a diagnosis of Diabetic Polyneuropathy (DPN), confirmed by clinical examination and electrophysiological testing.
  • Participants must have stable glycemic control for at least three months prior to enrollment.
  • Individuals must be able to walk independently, with or without the use of an assistive device.

Exclusion criteria

Exclusion Criteria:

  • Individuals with severe visual or vestibular impairments are excluded from participation.
  • Participants with significant musculoskeletal disorders affecting gait are not eligible.
  • Individuals with severe cardiovascular or respiratory conditions are excluded.
  • Participants with cognitive impairments that prevent active participation are not eligible.
  • Individuals currently engaged in structured physical therapy or balance training programs are excluded.
05

Study design

Phase
Phase 1
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Investigator)
Enrollment
24 participants (estimated)

Study arms

  • Experimental
    The Feldenkrais-based intervention

    this group recieve The Feldenkrais-based intervention consisted of guided awareness exercises

    Other: The Feldenkrais-based intervention

  • Active comparator
    a conventional balance training program

    The control group participated in a conventional balance training program consisting of static and dynamic balance exercises, gait training, and strength-building activities, matched for session frequency and duration

Interventions

  • OtherThe Feldenkrais-based intervention

    The Feldenkrais-based intervention consisted of guided awareness exercises aimed at improving movement patterns, proprioception, and postural control. Sessions were conducted twice weekly for 12 weeks, with each session lasting approximately 45 minutes

  • Otherconventional balance training program

    a conventional balance training program consisting of static and dynamic balance exercises, gait training, and strength-building activities, matched for session frequency and duration

06

What researchers measure

Primary outcomes

  1. Dynamic Balance

    Assessed using the Timed Up and Go Test, which measures the time taken to stand from a seated position, walk three meters, turn around, walk back, and sit down.

    Time frame: From enrollment to the end of treatment at 12 weeks

  2. Postural Control

    Evaluated using the Biodex Balance System, which measures limits of stability and sway index

    Time frame: From enrollment to the end of treatment at 12 weeks

  3. Fear of Falling

    Assessed using the Falls Efficacy Scale, a self-reported measure of confidence in performing daily activities without falling.

    Time frame: From enrollment to the end of treatment at 12 weeks

07

Study locations

1 site
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Start is estimated for Mar 2025; primary completion for Apr 2025, 1 month later.

How these figures are worked out, and which studies are left out of them.

Registered
Feb 5, 2025
First posted
Apr 1, 2025
StartEst.
Mar 30, 2025
Primary completionEst.
Apr 30, 2025
CompletionEst.
Jun 30, 2025
Last update
Apr 1, 2025
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Apr 1, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06904417
Lead sponsor
Cairo University
Responsible party
Islam Hassan Fayed (Physiotherapist, Cairo University) — Principal investigator
First posted
Apr 1, 2025
Start date
Mar 30, 2025 (estimated)
Primary completion
Apr 30, 2025 (estimated)
Completion
Jun 30, 2025 (estimated)
Last update
Apr 1, 2025

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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