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Peroneal NeuropathyNCT07191301

Functional Strength Training and Kinesiotaping, With and Without Proprioceptive Neuromuscular Facilitation in Fibular (Peroneal) Neuropathy

A study testing Functional Strength Training, Kinesio Taping, and Proprioceptive Neuromuscular Facilitation and Functional Strength Training and Kinesio Taping in people with Peroneal Neuropathy, run by University of Lahore at 1 site in Pakistan.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Fibular neuropathy frequently manifests as foot drop, muscle weakness, altered gait, and sensory loss, all of which severely reduce mobility and quality of life. There is still uncertainty regarding the efficacy of kinesio taping (KT), proprioceptive neuromuscular facilitation (PNF), and functional strength training… Read more about this study

Who is it for?
Ages 18 to 35 years
Conditions the study is for
Peroneal Neuropathy
What is being tested?
Functional Strength Training, Kinesio Taping, and Proprioceptive Neuromuscular Facilitation and Functional Strength Training and Kinesio Taping
Could I receive a placebo?
No, everyone receives an active treatment
How many people
48 participants
Where
1 sitePakistan
Study dates
10 Aug 2025to 30 Dec 2025
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 35 years
  • All sexes
  • No healthy volunteers
  • Adult

Who may be able to join

  • • Adults (18-35 years old) are diagnosed with fibular neuropathy due to trauma or compression.
  • Patients with muscle weakness, impaired balance and abnormal gait.
  • Both Male and female participants will be included.
  • Patients who test positive to the drag or slap test will be considered positive if the patient have difficulty in lifting the forefoot while walking, leading to dragging of the toes or compensatory hip/knee movements.

Who cannot join

  • • Recent foot or ankle surgery (<6 months).
  • Complete loss of nerve supply
  • Severe musculoskeletal or neurological conditions (Amyotrophic lateral sclerosis, multiple sclerosis, myopathies, severe osteoarthritis, severe compression, progressive neuropathies, severe balance and fall risk, Guillain-Barré Syndrome (GBS) and peripheral vascular diseases).
  • Allergies to Kinesio tape materials.
  • Patients who are not psychologically fit such as those who have undergone trauma and patients with severe psychological disorders (major depressive disorder, PTSD, schizophrenia) will be excluded if they have had a diagnosis within the last 6 months.

Trial locations and contacts

1 site in 1 country.

Pakistan1 site
  • UIPT, UOL, Lahore

    Lahore

Other trials in Pakistan

About this study

Official title: "Functional Strength Training and Kinesiotaping With and Without Proprioceptive Neuromuscular Facilitation Technique in Fibular (Peroneal) Neuropathy"

Fibular neuropathy frequently manifests as foot drop, muscle weakness, altered gait, and sensory loss, all of which severely reduce mobility and quality of life. There is still uncertainty regarding the efficacy of kinesio taping (KT), proprioceptive neuromuscular facilitation (PNF), and functional strength training (FST) in combination. Although PNF improves neuromuscular coordination, KT provides proprioceptive input, and FST increases strength and mobility, there are no set treatment guidelines and little research has compared these modalities. In order to contribute to evidence-based rehabilitation techniques for people with fibular neuropathy, this study attempts to assess whether adding PNF to FST and KT improves functional outcomes compared to FST and KT alone.

Being tested
Functional Strength Training, Kinesio Taping, and Proprioceptive Neuromuscular Facilitation, Functional Strength Training and Kinesio Taping
Medical subject headings
Peroneal Neuropathies

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Functional Strength Training, Kinesio Taping, and Proprioceptive Neuromuscular FacilitationBehavioural

    Participants will undergo 8 weeks of supervised treatment, 3 sessions per week (24 sessions). Each session includes a warm-up with stretches, range-of-motion exercises, and Functional Strength Training (mini hops, stair climbing, ramp walking, sit-to-stand). Kinesio Taping will be applied from the foot's dorsum along the tibialis anterior and peroneus longus with 25-50% stretch for ankle support and dorsiflexor facilitation, re-applied every 3-4 days. In addition, Proprioceptive Neuromuscular Facilitation (PNF) lower-limb D1 flexion/extension patterns with manual resistance will be performed in 3 sets of 5 repetitions, lasting 35-40 minutes per session.

  • Functional Strength Training and Kinesio TapingBehavioural

    Participants will undergo 8 weeks of supervised treatment, 3 sessions per week (24 sessions). Each session includes a warm-up with stretches, range-of-motion exercises, and Functional Strength Training (mini hops, stair climbing, ramp walking, sit-to-stand). Kinesio Taping will be applied from the foot's dorsum along the tibialis anterior and peroneus longus with 25-50% stretch for ankle support and dorsiflexor facilitation, re-applied every 3-4 days. No PNF techniques will be applied.

Study groups in NCT07191301
Study groupRoleWhat they receive
Interventional Group AExperimentalFunctional Strength Training (FST) + Kinesio Taping (KT) with Proprioceptive Neuromuscular Facilitation (PNF).
Receives: Behavioral: Functional Strength Training, Kinesio Taping, and Proprioceptive Neuromuscular Facilitation; Behavioral: Functional Strength Training and Kinesio Taping
Control Group BActive comparatorFunctional Strength Training (FST) + Kinesio Taping (KT) without PNF.
Receives: Behavioral: Functional Strength Training, Kinesio Taping, and Proprioceptive Neuromuscular Facilitation; Behavioral: Functional Strength Training and Kinesio Taping

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change in dorsiflexor muscle strength measured by Manual Muscle Grading (MMG)

    Measured: Baseline (Week 0), Mid-point (Week 4), and Post-intervention (Week 8)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted24 Sep 2025
  2. Study start10 Aug 2025
  3. Primary completion10 Dec 2025
  4. Study completion30 Dec 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
48 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07191301
Sponsor's protocol ID
Sumayah Farooq
Status last verified
Mar 2026
First submitted
17 Sep 2025
Last updated
5 Mar 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Functional Strength Training, Kinesio Taping, and Proprioceptive Neuromuscular Facilitation and Functional Strength Training and Kinesio Taping in people with Peroneal Neuropathy, run by University of Lahore at 1 site in Pakistan.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 5 Mar 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Pakistan. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change in dorsiflexor muscle strength measured by Manual Muscle Grading (MMG) (time frame: Baseline (Week 0), Mid-point (Week 4), and Post-intervention (Week 8)). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 5 Mar 2026.

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