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CompletedNCT07616661FEToG-DPNUpdated Sep 10, 2026

Feldenkrais vs. Task Oriented Gait Training on Diabetic Peripheral Neuropathy

An interventional study of Feldenkrais Exercises and Task Oriented Gait Training in Diabetic Peripheral Neuropathy, sponsored by University of Faisalabad. Completed at 1 site in Pakistan. Open to participants aged 45 Years to 55 Years. Per ClinicalTrials.gov, last updated 2026-09-10.

Sponsored by University of Faisalabad · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 3 months after the study started (first participant enrolled Feb 2026, registered May 2026).
Phase
Not applicable
Study type
Interventional
Enrollment
40
Allocation
Randomized
Ages
45 Years to 55 Years
Sex
All
01

Study summary

Diabetic Peripheral Neuropathy (DPN) causes balance problems, falls, and sensory loss in the feet. This study compares two non-drug exercise programs to see which works better. The first program is Feldenkrais exercises, which focus on movement awareness and retraining the brain. The second program is Task Oriented Gait Training, which practices specific walking tasks. Researchers will measure balance, joint position sense, touch sensation, fear of falling, and quality of life. Forty participants will be split into two groups. The study will last 12 weeks.

Read the detailed description

This study is a single-blinded, randomized clinical trial. Forty participants with Diabetic Peripheral Neuropathy (DPN) will be recruited from Shahid Heera's Health Clinic and Madinah Teaching Hospital in Faisalabad. Participants will be screened using the Michigan Neuropathy Screening Instrument (MNSI). Inclusion criteria include participants aged 45-55 years with type 1 or type 2 diabetes, a history of at least one fall in the past six months, a body mass index between 18.5 and 29.9, controlled blood glucose levels, and a Berg Balance Scale score between 21 and 40. Participants will be excluded if they have foot ulcers, lower leg amputation, Charcot foot, retinopathy, hypertension, or are already receiving rehabilitation.

Eligible participants will be randomly allocated into two groups of twenty using a computer-generated method. Group A will receive Feldenkrais exercises. Group B will receive Task Oriented Gait Training. Both groups will attend two sessions per week for twelve weeks. Each session lasts sixty minutes, consisting of a ten-minute warm-up, a forty-to-forty-five-minute main exercise session, and a ten-minute cool-down. Outcome measures will be recorded at baseline, the sixth week, and the twelfth week. The primary outcome measures are static and dynamic balance (Berg Balance Scale), ankle joint proprioception (joint position sense test), and tactile sensation (monofilament test). The secondary outcome measures are somatosensory postural control (Cumulative Somatosensory Impairment Index), fear of falling (Fall Efficacy Scale), self-awareness learning (educational brochure), and quality of life (SF-36 Questionnaire). SPSS version 20 will be used for statistical analysis.

02

Conditions studied

  • Diabetic Peripheral Neuropathy

Keywords

  • Feldenkrais
  • Task Oriented Gait Training
  • Balance
  • Proprioception
  • Neuropathy
03

In context

Lead sponsor

University of Faisalabad is the lead sponsor of 83 studies on the registry; 26 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
45 Years to 55 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Age ranges from 45-55 years
  • Diagnosed type 1 and type 2 diabetes
  • Suffered from a fall in last 6 months
  • MNSI Questionnaire scored > 2/13
  • MNSI physical assessment scored > 4/10
  • BMI = 18.5 - 29.9
  • Controlled blood glucose level
  • Berg Balance scale = 21-40
  • Willingness to participate and provide consent

Exclusion criteria

Exclusion Criteria:

  • Presence of ulcers at foot
  • Lower leg amputation
  • Charcot foot
  • Retinopathy
  • Hypertension
  • Already receiving rehabilitation
  • History of trauma or fracture
  • Any related orthopedic conditions
  • CVS related conditions
  • Autonomic neuropathy
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
40 participants (actual)

Study arms

  • Experimental
    Feldenkrais Exercises

    Participants perform Feldenkrais exercises for 40 minutes per session, focusing on somatosensory re-education, axial movements, and balance.

    Other: Feldenkrais Exercises · Other: baseline warm up and cool down Exercises

  • Active comparator
    Task Oriented Gait Training

    Participants perform Task Oriented Gait Training for 45 minutes per session, focusing on functional tasks like walking on surfaces, changing directions, and obstacle negotiation.

    Other: Task Oriented Gait Training · Other: baseline warm up and cool down Exercises

Interventions

  • OtherFeldenkrais Exercises

    This intervention includes 16 specific movement lessons (e.g., turning improvement, weight transference, sensing the feet, walking in tandem). The protocol is derived from Mazuelas et al. 2024. Sessions are 40 minutes, twice a week for 12 weeks, guided by a physiotherapist.

  • OtherTask Oriented Gait Training

    This intervention includes functional tasks such as walking with reduced base of support, obstacle crossing, and ramp walking. The protocol is derived from Salsabili et al. 2015. Sessions are 45 minutes, twice a week for 12 weeks.

  • Otherbaseline warm up and cool down Exercises

    Warm up exercises: Warm up exercises before the start of training exercises for about ten minutes. These include: • Leg swings (forward and backward) • Side to side leg swings • Leg kicks 20 reps/side • Standing on tip toes • Mild stretching Cool down exercises: Cool Down exercises after the end of training exercises for about ten minutes to induce relaxation. These include: • Deep breathing exercise • Abdominal breathing exercise • Leg swings • Standing on tip toes • Mild stretching

06

What researchers measure

Primary outcomes

  1. Change in Berg Balance Scale Score

    The Berg Balance Scale (BBS) measures static and dynamic balance. It contains 14 items scored from 0 to 4. Total score ranges from 0 to 56. Higher scores indicate better balance.

    Time frame: Baseline, Week 6, Week 12

  2. Change in Ankle Joint Proprioception

    Measured using the Joint Position Sense Test (JPST) with a goniometer. The participant actively reproduces a target joint angle. The difference in degrees between the target and the reproduction is recorded. Smaller differences indicate better proprioception.

    Time frame: Baseline, Week 6, Week 12

  3. Change in Tactile Sensation

    Measured using the Semmes-Weinstein Monofilament (10g). The filament is applied to 10 sites on the plantar surface of the foot. The number of correctly detected applications out of 10 is recorded. Higher scores indicate better sensation.

    Time frame: Baseline, Week 6, Week 12

Secondary outcomes

  1. Change in Cumulative Somatosensory Impairment Index (CSII)

    Measures somatosensory postural control and functional awareness. Scale range and specific scoring will be calculated per the CSII manual.

    Time frame: Baseline, Week 6, Week 12

  2. Change in Fear of Falling

    Measured using the Fall Efficacy Scale (FES). Participants rate confidence in performing 10 activities without falling. Scores range from 10 (high confidence) to 100 (low confidence).

    Time frame: Baseline, Week 6, Week 12

  3. Change in Quality of Life

    Measured using the SF-36 Questionnaire. This tool assesses physical and mental health across 8 domains. Scores are transformed into a scale from 0 to 100. Higher scores indicate better quality of life.

    Time frame: Baseline, Week 6, Week 12

  4. Self-Awareness Learning Adherence

    Measured by the return of a structured educational brochure checklist. Participants report if they performed prescribed home self-learning activities.

    Time frame: Week 12

07

Study locations

1 site
  • The University of Faisalabad
    Faisalābad, Punjab Province 3800, Pakistan
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 10, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07616661
Lead sponsor
University of Faisalabad
Responsible party
Dr. Marium Zafar (Assistant Professor, Department of Rehabilitation Sciences, University of Faisalabad) — Principal investigator
First posted
Jun 1, 2026
Start date
Feb 1, 2026
Primary completion
Apr 1, 2026
Completion
May 28, 2026
Last update
Sep 10, 2026

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Sep 2026. You cannot join it, but the record below documents what was studied.

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