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Effectiveness of Pain Neuroscience Education Along With Neural Mobilization Versus Neural Mobilization Alone on Pain, Functional Disability And Quality of Life In Patients With Diabetic Neuropathic Pain

ConditionDiabetic Neuropathic Pain
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age40+
SponsorIbadat International University, Islamabad

About this trial

This is a randomized controlled trial aims to evaluate the comparative effect of Pain Neuroscience Education combined with neural mobilization versus neural mobilization alone in patients with diabetic neuropathic pain. This study will Compare pain intensity between intervention groups and assess functional disability outcomes. Furthermore, this will evaluate changes in quality of life and to analyze pain-related beliefs following PNE.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

None

Disqualifiers

None

Trial design

Design model

Parallel

Treatments tested in this trial

  • Pain Neurosciences Education + Neural Mobilization

    Other intervention

    In Group A pain neuroscience Education will be given in adjunct with neural mobilization techniques Target nerves: Sciatic, tibial \& common peroneal Technique: Slider neurodynamic mobilization Dosage: 10-15 reps × 2-3 sets \| Rest: 30-60 sec between sets Session duration: 15-20 minutes PNE: 20-30 min (weeks 1-2) → 10 min reinforcement (weeks 3-6) Methods: Simple diagrams, patient-friendly metaphors, video demonstrations

Treatment groups

40 Participants
are divided into 2 treatment groups
Group A: Group A - Pain Neurosciences Education combined with Neural MobilizationExperimental treatment 1 intervention
Group B: Group B - Neural Mobilization AloneActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Pain intensity

Pain intensity will be evaluated using Numeric Pain Rating Scale

Time frame
Baseline to week 6
2

Functional disability

Functional disability will be evaluated using Urdu version of Lower Extremity Functional Scale (LEFS)

Time frame
Baseline to week 6
3

Quality of life

Quality of life will be evaluated by World Health Organization Quality Of Life-BREF

Time frame
Baseline to week 6
4

Central sensitization

Central sensitization will be evaluated using Central Sensitization Inventory

Time frame
Baseline to week 6

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Ibadat International University, Islamabad

Lead sponsor

Source ClinicalTrials.gov

This trial is not recruiting at the moment. You can still explore other options: