NCT07066670

Brief Summary

This study aimed to evaluate the comparative effects of Strain Counterstrain (SCS) and Muscle Energy Technique (MET) on pain, range of motion (ROM), and functional disability in patients with knee osteoarthritis (KOA). Conducted as a single-blinded randomized control trial at the University of Lahore Teaching Hospital, 76 participants were divided into two groups, receiving either SCS or MET alongside routine physical therapy. Outcome measures included pain intensity, ROM, and functional disability via KOOS.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
76

participants targeted

Target at P50-P75 for not_applicable stroke

Timeline
Completed

Started Mar 2024

Shorter than P25 for not_applicable stroke

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

March 15, 2024

Completed
9 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 13, 2024

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

February 20, 2025

Completed
1 month until next milestone

First Submitted

Initial submission to the registry

April 3, 2025

Completed
3 months until next milestone

First Posted

Study publicly available on registry

July 15, 2025

Completed
Last Updated

July 15, 2025

Status Verified

April 1, 2025

Enrollment Period

9 months

First QC Date

April 3, 2025

Last Update Submit

July 4, 2025

Conditions

Keywords

Knee OsteoarthritisStrain CounterstrainMuscle Energy TechniquePain ManagementFunctional Disability

Outcome Measures

Primary Outcomes (1)

  • Pain intensity reduction measured by Numeric Pain Rating Scale (NPRS)

    Pain intensity was assessed using the Numeric Pain Rating Scale (NPRS), a validated 0-10 scale where 0 indicates "no pain" and 10 indicates "worst possible pain." Assessments were conducted at baseline, 4 weeks, and 8 weeks. A lower score represents improvement.

    Baseline, Week 4, and Week 8

Secondary Outcomes (2)

  • Improvement in range of motion (ROM) measured using goniometry

    Baseline, Week 4, and Week 8

  • Change in functional disability measured by KOOS questionnaire

    Baseline, Week 4, and Week 8

Study Arms (2)

Strain Counterstrain with Routine Physical Therapy

EXPERIMENTAL

Participants in this arm received Strain Counterstrain (SCS) along with routine physical therapy. SCS involved identifying and holding tender points in positions of comfort for 90 seconds to relieve pain and improve range of motion. Routine physical therapy included TENS, infrared therapy, ultrasound, strengthening exercises (short arc quads, seated knee flexion/extension, terminal knee extension), and stretching exercises (straight leg raises, lying and sitting hamstring stretches). The intervention was delivered 5 days a week for 8 weeks. Education on weight management and joint protection strategies was also provided.

Behavioral: Strain Counterstrain with Routine Physical Therapy

Muscle Energy Technique with Routine Physical Therapy

EXPERIMENTAL

Participants in this arm received Muscle Energy Technique (MET) along with routine physical therapy. MET involved post-isometric relaxation and slow eccentric isotonic stretching techniques targeting hamstrings and quadriceps, helping to restore joint mobility and muscle flexibility. Routine physical therapy included TENS, infrared therapy, ultrasound, strengthening exercises (short arc quads, seated knee flexion/extension, terminal knee extension), and stretching exercises (straight leg raises, lying and sitting hamstring stretches). The intervention was administered 5 days per week over 8 weeks, along with patient education on lifestyle and joint care.

Behavioral: Muscle Energy Technique with Routine Physical Therapy

Interventions

This intervention involves applying the Strain Counterstrain (SCS) technique in combination with standard physical therapy. SCS targets tender points through passive positioning to reduce muscle tension and pain. The patient is positioned in a position of comfort for 90 seconds while monitoring the tender point. This is followed by gradual return to neutral. Routine physical therapy includes electrotherapy (TENS, IR, ultrasound), strengthening (short arc quads, terminal knee extension), and stretching exercises. The therapy is administered 5 days per week over 8 weeks.

Strain Counterstrain with Routine Physical Therapy

This intervention combines Muscle Energy Technique (MET) with routine physical therapy. MET involves voluntary muscle contractions against resistance, followed by stretching to restore range of motion and relieve pain. Techniques include post-isometric relaxation and slow eccentric isotonic stretching, particularly targeting hamstring and quadriceps tightness. Routine physical therapy includes electrotherapy (TENS, IR, ultrasound), as well as structured strengthening and stretching exercises. The intervention was delivered 5 days a week for 8 weeks.

Muscle Energy Technique with Routine Physical Therapy

Eligibility Criteria

Age45 Years - 65 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Age between 45 to 65 years (Pandiselvi, 2019).
  • Patients who were willing and able to comply with the study protocol and follow-up procedures (Arslan et al., 2022).
  • Patients having Grade 2 knee OA Kellgren and Lawrence system. In this system, grade 2 signifies minimal severity of OA (Ratzlaff et al., 2018).

You may not qualify if:

  • Congenital deformities (Deng et al., 2021).
  • Having any tumor or related pathology such as cancer (Arslan et al., 2022).
  • Patients having any previous knee surgery (Khan et al., 2023).
  • Patients with isolated/predominantly patellofemoral symptomatic osteoarthritis, inflammatory diseases, joint effusion, or excessive knee deformity (Deng et al., 2021).

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

The University of Lahore Teaching Hospital

Lahore, 54590, Pakistan

Location

Related Publications (1)

  • Ratzlaff C, Ashbeck EL, Guermazi A, Roemer FW, Duryea J, Kwoh CK. A quantitative metric for knee osteoarthritis: reference values of joint space loss. Osteoarthritis Cartilage. 2018 Sep;26(9):1215-1224. doi: 10.1016/j.joca.2018.05.014. Epub 2018 May 26.

    PMID: 29842940BACKGROUND

MeSH Terms

Conditions

StrokeOsteoarthritis, KneeAgnosia

Condition Hierarchy (Ancestors)

Cerebrovascular DisordersBrain DiseasesCentral Nervous System DiseasesNervous System DiseasesVascular DiseasesCardiovascular DiseasesOsteoarthritisArthritisJoint DiseasesMusculoskeletal DiseasesRheumatic DiseasesPerceptual DisordersNeurobehavioral ManifestationsNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Masking Details
Only the outcomes assessor was blinded to the participants' group assignments to ensure objective measurement of pain, ROM, and functional disability scores.
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: Two-arm parallel design where each group receives a distinct manual therapy intervention (SCS or MET) along with standardized physiotherapy. The study tracks changes in pain, ROM, and disability over 8 weeks.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Student

Study Record Dates

First Submitted

April 3, 2025

First Posted

July 15, 2025

Study Start

March 15, 2024

Primary Completion

December 13, 2024

Study Completion

February 20, 2025

Last Updated

July 15, 2025

Record last verified: 2025-04

Data Sharing

IPD Sharing
Will not share

Locations