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Effects of Corrective Exercise Training for Improving Neuropathic Pain and Function in Knee Osteoarthritis

Effects of Corrective Exercise Training for Improving Neuropathic Pain and Function in Knee Osteoarthritis

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04995250
Enrollment
16
Registered
2021-08-06
Start date
2020-04-01
Completion date
2020-12-30
Last updated
2021-09-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Osteoarthritis, Knee

Keywords

Knee osteoarthritis

Brief summary

Patients with neuropathic pain had longer duration of symptoms increased severity of pain, functional limitation and disability as compare to the patient with general knee osteoarthritis. Objective: To find out the effects of corrective exercise training for improving neuropathic pain and function in knee OA patients.

Detailed description

This study was a Quasi experimental study. It was conducted at Horizon Hospital Johar Town Lahore. The study was completed in Six months. Consecutive sampling technique was used to collect the data. The sample size of 16 patients was taken in this study to find out the effects of corrective exercises training for improving neuropathic pain and function in patients with knee osteoarthritis. For descriptive analysis we used frequency, percentages and charts. For quantitative measure. Repeated Measured ANOVA was used.

Interventions

OTHERcorrective exercise training for knee

All patients received 12 weeks (3 days per week) physiotherapy sessions with hot pack, TENS and Ultrasound session for 10 mints and knee isometric, quad strengthening, adductor and abductor strengthening, calf stretch, hamstring stretch, Maitland mobilization, Unconventional Corrective knee exercise protocol treatment: standing on one extremity, up and down on bosu exercise, walking to lateral direction, walking to anterio-posterior direction, walking to anterio-posterior and lateral for 20 mints. Data were collected at baseline, at week 4 and at post treatment (week 12).

Sponsors

Riphah International University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* ACR Criteria for osteoarthritis * Neuropathic pain * Age over 65 * DN4 cut off value is 4/10 * Less than 30 minutes of morning stiffness * Grade I and II * Crepitus on active motion * Bony tenderness * Bony enlargement * No palpable warmth of synovium

Exclusion criteria

* Knee complain that require urgent medical attention (fracture and infection) * Diabetes mellitus * Patients with malignancies * Neurological disorders * Systematic musculoskeletal diseases (Parkinson's, rheumatoid arthritis etc) * Incapability of understanding implication of participants

Design outcomes

Primary

MeasureTime frameDescription
Western Ontario and McMaster Osteoarthritis Index6 months0-100, 0 means no disability 100 means maximum disability
Numeric pain rating scale6 months0-10,no pain and the worse pain, on an 11 point scale
Douleur Neuropathique 4 Questionnaire6 monthsThe total score is calculated as the sum of 10 items and the cut off value for the diagnosis of neuropathic pain is a total score of 4/10

Countries

Pakistan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026