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RecruitingNCT07396233Updated Feb 11, 2026

Effects of Diagonal Proprioceptive Neuromuscular Facilitation Patterns on Pain and Functional Outcomes in Patients With Knee Osteoarthritis

An interventional study of Diagonal Proprioceptive Neuromuscular Facilitation (PNF) Pattern Exercises and Conventional Strength Training Exercises in Knee Osteoarthristis, Osteearthritis and Knee Pain Arthritis, sponsored by University of Karachi. Recruiting at 2 sites in Pakistan. Open to participants aged 40 Years to 60 Years. Per ClinicalTrials.gov, last updated 2026-02-11.

Sponsored by University of Karachi · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
150
Allocation
Randomized
Ages
40 Years to 60 Years
Sex
All
01

Study summary

A randomized controlled trial will be conducted at the Department of Physiotherapy, Dr. Ziauddin Hospital and Al-Rayaz Hospital, Karachi, Pakistan. A total of 150 patients diagnosed with knee osteoarthritis, aged between 40-60 years, will be recruited through a non-probability purposive sampling technique. Written informed consent will be obtained from all eligible participants prior to enrollment. The participants will be randomly allocated by the help of computer generated randomization sheet, into two groups i.e. experimental and the control group, with 75 participants in each group. Group A (experimental group) will receive diagonal proprioceptive neuromuscular facilitation (PNF) pattern exercises, while Group B (control group) will receive conventional strength training exercises. Heat therapy will be administered to both groups. All participants will be assessed using a standardized assessment form. Outcome measures will include pain intensity, knee range of motion, functional disability, hamstring flexibility, dynamic balance, and fatigue level. A single blinded assessor will assess all participants at baseline and at post intervention. Treatment sessions will be given thrice a week on alternate days for 6 weeks.

Read the detailed description

The Statistical Package for the Social Sciences (SPSS) version 23 will be used for data analysis. Mean and standard deviation will be calculated for quantitative variables such as age. Qualitative variables will be presented as frequencies and percentages. Outcome measures (decrease pain intensity, improve functional disability, increase knee range of motion, improve hamstring flexibility, dynamic balance, and fatigue level) recorded at baseline and after 18th session of intervention will be compared and analyzed. Repeated measures ANOVA will be applied for statistical analysis. A p-value of less than 0.05 will be considered as the level of statistical significance.

02

Conditions studied

  • Knee Osteoarthristis
  • Osteearthritis
  • Knee Pain Arthritis

Keywords

  • Knee Osteoarthritis
  • Functional Disability
  • Knee Pain
  • Conventional Training
  • Osteoarthritis
  • Arthritis
  • Musculoskeletal Disease
  • Joint Disease
03

Who can participate

Ages eligible
40 Years to 60 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Both male and females with an age range between 40-60 years.
  • Patients diagnosed with unilateral or bilateral Knee OA.
  • Grade-II or grade-III on kellgren and Lawrence classification.
  • Patients having pain intensity more than 3.4 cm on VAS as minimum cut off value.
  • Duration of knee OA more than 3 months (chronic).

Exclusion criteria

Exclusion Criteria:

  • Patients with any neurological disorder.
  • History of lower limb arthroplasty or any other knee surgery.
  • Septic knee arthritis.
  • Inflammatory rheumatic disease such as rheumatoid arthritis and gout.
  • Cancer or any other malignancy such as bone tumor.
  • Knee deformities such as contracture, genu valgum and genu varum.
  • History of ligamentous injury and meniscal tear.
04

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
150 participants (estimated)

Study arms

  • Experimental
    Diagonal Proprioceptive Neuromuscular Facilitation (PNF) Pattern Exercises + Heat Therapy.

    This arm will receive PNF pattern exercises using Diagonal 1 and Diagonal 2 Lower Limb Patterns of PNF and the heat therapy

    Other: Diagonal Proprioceptive Neuromuscular Facilitation (PNF) Pattern Exercises · Other: Heat Therapy

  • Active comparator
    Conventional Strength Training Exercises + Heat Therapy

    This arm will receive evidence based treatment of Quadripceps and Hip Abductor Strengthening exercises and the heat therapy.

    Other: Conventional Strength Training Exercises · Other: Heat Therapy

Interventions

  • OtherDiagonal Proprioceptive Neuromuscular Facilitation (PNF) Pattern Exercises

    Diagonal PNF pattern exercises include Diagonal 1 and Diagonal 2 lower limb pattern movements performed against resistance to improve strength, flexibility, and functional performance.

  • OtherConventional Strength Training Exercises

    The conventional strength training exercises include quadriceps and hip abductor strengthening performed using resisted active movements to improve muscle strength and functional ability.

  • OtherHeat Therapy

    Heat therapy will be given for 10 minutes by the help of electric heating pad.

05

What researchers measure

Primary outcomes

  1. Change in pain intensity will be assessed with Visual Analogue Scale

    The Visual Analogue Scale is a unidimensional measure of pain intensity, used to record patients' pain progression, or assess pain severity in different conditions. It is 0 to 10 cm scale. Patients rate their pain on the scale. Higher the score in centimeter, severe will be the pain experienced.

    Time frame: Baseline and after 6 weeks of intervention

  2. Change in range of motion will be assessed with Universal Goniometer

    The universal goniometer is an instrument for the precise measurement of range of movement angles in degree, especially one used to measure the angles before and after range of motion. Increase in the degree of angle suggests increase in range of movement.

    Time frame: Baseline and after 6 weeks of intervention.

Secondary outcomes

  1. Change in functional disability will be assessed with Knee Injury and Osteoarthritis Outcome Score (KOOS)

    The Knee Injury and Osteoarthritis Outcome Score (KOOS) is a knee-specific instrument, developed to assess the patients' opinion about their knee and associated problems regarding functional disability. It consists of total 100 scores. Increase in scores suggests better function and decrease in scores suggests increased functional disability.

    Time frame: Baseline and after 6 weeks of intervention.

  2. Change in hamstring flexibility will be assessed with Active Knee Extension test.

    The Active Knee Extension (AKE) test will be used to assess hamstring muscle length using a goniometer with the hip flexion position at 90°. A greater knee extension angle indicates greater hamstring muscle length.

    Time frame: Baseline and after 6 weeks of intervention.

  3. Change in dynamic balance will be assessed with Four Step Square Test (FSST)

    The Four Square Step Test will be used to assess dynamic balance. It is measured in seconds. A higher completion times indicate poorer dynamic balance and a greater risk of falls.

    Time frame: Baseline and after 6 weeks of intervention.

  4. Change in fatigue level will be assessed with Multidimensional Fatigue Inventory questionnaire.

    The multidimensional fatigue inventory is a 20-item scale designed to evaluate five dimensions of fatigue: general fatigue, physical fatigue, reduced motivation, reduced activity, and mental fatigue. Higher total scores correspond with more acute levels of fatigue.

    Time frame: Baseline and after 6 weeks of intervention.

06

Study locations

2 of 2 sites recruiting
  • Al-Rayaz Hospital
    Karachi, Sindh 74600, Pakistan
    Recruiting
  • Dr. Ziauddin Hospital
    Karachi, Sindh 74600, Pakistan
    Recruiting
07

References and documents

Publications

  • Nafees K, Baig AAM, Ali SS, Ishaque F. Dynamic soft tissue mobilization versus proprioceptive neuromuscular facilitation in reducing hamstring muscle tightness in patients with knee osteoarthritis: a randomized control trial. BMC Musculoskelet Disord. 2023 Jun 2;24(1):447. doi: 10.1186/s12891-023-06571-y. PubMed 37268961 ↗
  • Gao B, Li L, Shen P, Zhou Z, Xu P, Sun W, Zhang C, Song Q. Effects of proprioceptive neuromuscular facilitation stretching in relieving pain and balancing knee loading during stepping over obstacles among older adults with knee osteoarthritis: A randomized controlled trial. PLoS One. 2023 Feb 13;18(2):e0280941. doi: 10.1371/journal.pone.0280941. eCollection 2023. PubMed 36780435 ↗
  • Geng R, Li J, Yu C, Zhang C, Chen F, Chen J, Ni H, Wang J, Kang K, Wei Z, Xu Y, Jin T. Knee osteoarthritis: Current status and research progress in treatment (Review). Exp Ther Med. 2023 Aug 25;26(4):481. doi: 10.3892/etm.2023.12180. eCollection 2023 Oct. PubMed 37745043 ↗
  • Song Q, Shen P, Mao M, Sun W, Zhang C, Li L. Proprioceptive neuromuscular facilitation improves pain and descending mechanics among elderly with knee osteoarthritis. Scand J Med Sci Sports. 2020 Sep;30(9):1655-1663. doi: 10.1111/sms.13709. Epub 2020 Jun 1. PubMed 32407583 ↗

Individual participant data

Plan to share: No — Results will be published by the investigators in academic journals. Sharing of generated study data will be carried out in several different ways. We plan to make our results available to researchers and potential collaborators interested in physical medicine rehabilitation and knee osteoarthritis management.

08

Registry details

Key details

Study ID
NCT07396233
Lead sponsor
University of Karachi
Responsible party
Rabia Hassan (Principal Investigator, University of Karachi) — Principal investigator
First posted
Feb 9, 2026
Start date
Feb 7, 2026
Primary completion
Jan 19, 2027 (estimated)
Completion
Feb 22, 2027 (estimated)
Last update
Feb 11, 2026

Study contacts

Rabia Hassan, MSAPT
Contact
rabiahassan096@gmail.com
+923345448859
Basit Ansari, PhD
Contact
basitansari@hotmail.com
+923222279221
Rabia Hassan, MSAPT
principal investigator · Ziauddin University
Basit Ansari, PhD
study chair · University of Karachi
Aftab Ahmed Mirza Baig, PhD
study director · IQRA University

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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