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RecruitingNCT07452081EMGUpdated Mar 5, 2026

Combined Effect of Sensory-motor Integration in Individuals With Postmenopausal Polyneuropathy

An interventional study of sensory motor integration and traditional excercises in Sensory-Motor Axonal Neuropathy, sponsored by New Ismailia National University. Recruiting at 2 sites in 2 countries. Open to female participants aged 45 Years to 55 Years. Per ClinicalTrials.gov, last updated 2026-03-05.

Sponsored by New Ismailia National University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by May 2026, 6 months ago, but the record still lists the study as recruiting.
  • Started Feb 2026; still recruiting 9 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
100
Allocation
Randomized
Ages
45 Years to 55 Years
Sex
Female
01

Study summary

Detect the combined effect of sensory-motor integration in individuals with postmenopausal polyneuropathy

Read the detailed description

This reach aim to conduct to improve balance and reduce pain in patients with post-menopausal with peripheral neuropathy

02

Conditions studied

  • Sensory-Motor Axonal Neuropathy
03

In context

Lead sponsor

New Ismailia National University is the lead sponsor of 8 studies on the registry; 4 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
Female
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

  • polyneuropathy pos-tmaneuposal
  • Type II Diabetes Mellitus
  • Suffering from numbness in upper and lower limbs for more than 4 months

Exclusion criteria

Exclusion Criteria:

  • hysterectomy
  • tumors
  • antidepressant dugs
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
100 participants (estimated)

Study arms

  • Experimental
    Group A

    has received Sensory Motor Integration was given in the form of tactile stimulation, thermal stimulation and proprioceptive stimulation as well as motor integration was given in the form of strengthening exercises and pelvic rocking training for 6 weeks

    Other: sensory motor integration

  • Active comparator
    Broup B

    will recieve conventional exercises in the form of Free exercises and gymnasium exercises of Upper limb and Lower limb along with 20 minutes walking

    Other: traditional excercises

Interventions

  • Othersensory motor integration

    pelvic rocking training and strengthening exercises

    Also known as: thermal, Tactile, and proprioceptive stimulation

  • Othertraditional excercises

    conventional

    Also known as: Free exercises and gymnasium exercises of Upper limb and Lower limb

06

What researchers measure

Primary outcomes

  1. pain intensity

    pain management will be evaluated by visual analogue scale with a minimum score of zero, and the maximum score is ten in addition, zero means a better score

    Time frame: 6 weeks

  2. balance assessment

    changes in balance parameters will be evaluated by the Biodex balance system that calculate the mediolateral stability index, anteroposterior stability index, and the overall. stability index.These indexes represent fluctuations around a zero point established before testing when the platform is stable. A high oSi score indicates poor balance, and the patient's maximum overall score would be 1.60.

    Time frame: 6 weeks

07

Study locations

2 of 2 sites recruiting
08

References and documents

Individual participant data

Plan to share: No — No IPD sharing

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 Mar 5, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07452081
Lead sponsor
New Ismailia National University
Responsible party
Mohamed Abdel Moeim Abo EL Ros (Assistant Professor of Pediatric Physical Therapy, Suez Canal University) — Principal investigator
First posted
Mar 5, 2026
Start date
Feb 1, 2026
Primary completion
May 1, 2026 (estimated)
Completion
Jun 1, 2026 (estimated)
Last update
Mar 5, 2026

Study contacts

Mohamed AM Abo El Ros
Contact
aboelroosmohamed61@gmail.com
01206530584
Mohamed AM Abo El Ros
Contact
mohamed.aboelros@pt.ninu.edu.eg
01206530584
Kerlos Kellini, Ph.D
study director · Al Zaytona University in Jordon

Oversight

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

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