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Effects of Proprioceptive Neuromuscular Training on Sensory and Motor Function in Guillain Barre Syndrome

R

Riphah International University

Status

Completed

Conditions

Guillain-Barre Syndrome

Treatments

Other: Proprioceptive Neuromuscular Training
Other: Conventional Physical Therapy

Study type

Interventional

Funder types

Other

Identifiers

NCT05491096
REC/22/0219 Salma

Details and patient eligibility

About

This study aims to determine the effects of Proprioceptive Neuromuscular Training on Sensory versus Motor Function in patients presenting with Guillain Barre Syndrome.

Full description

This study will be a randomized controlled trial and will be conducted to determine the effects of proprioceptive neuro-muscular training on sensory and motor function of lower limb,In this study data will be collected from multiple Hospitals of Lahore via Berg Balance Scale, Timed Up and Go test One Leg Stance test before and after intervention. Non- probability convenient sampling technique will be used to enroll 26 patients in total. The patients will be randomly allocated into two groups through lottery method, to either the proprioceptive training group or control group.Both groups will be assessed for proprioception via lower extremity position test as a baseline. Proprioception training programme will be implemented in experimental group and will be carried out for eight weeks, with three (60-minute) sessions per week. It will start with 10 minutes of Warm-up. This will be followed by 30 minutes of proprioceptive exercises targeting lower extremities. Proprioceptive exercises will be divided into three components, standing on Foam with eyes open and eyes closed and passing any object from one subject to the other for 10 minutes, throwing and catching a ball will be performed while standing on foam for additional 10 minutes, throwing and catching a ball, will be performed on trampoline to further challenge the balance system. After each set of 10-minute exercise, the subjects will be given two-minute resting periods. In the end, 10 minutes will be given for cool down exercises to bring the heart rate back to resting level. All participants in both groups will be evaluated before and after the treatment programs. Data will be analyzed by using Statistical Package of Social Sciences Version 26.

Enrollment

26 patients

Sex

All

Ages

10 to 25 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Diagnosed with Guillain Barre Syndrome already taking treatments
  2. Inflammatory Demyelinating Guillain Barre Syndrome patients
  3. Acute motor sensory axonal neuropathy
  4. Guillain Barre Syndrome patients in the subacute phase
  5. Guillain Barre Syndrome patients with impaired proprioception
  6. Patients with Glasgow Coma Scale above 12

Exclusion criteria

  1. Other Guillain Barre Syndrome types
  2. Spinal cord injury
  3. Traumatic neuritis
  4. Not Fulfilling Above Criteria Of Age

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

26 participants in 2 patient groups, including a placebo group

Proprioceptive Neuromuscular Training
Experimental group
Description:
It consists of 13 patients who will receive conventional exercises and proprioceptive training with 2 sessions per week for 8 weeks.
Treatment:
Other: Proprioceptive Neuromuscular Training
Conventional Physical Therapy
Placebo Comparator group
Description:
It consists of 13 patients who will receive conventional exercises i.e; strengthening exercises, 2 sessions per week for 8 weeks
Treatment:
Other: Conventional Physical Therapy

Trial contacts and locations

1

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Central trial contact

Imran Amjad, Phd

Data sourced from clinicaltrials.gov

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