NCT07628426

Brief Summary

This single-blinded randomized clinical trial aims to evaluate the comparative effects of Myokinetic Stretching Technique (MST) alone versus MST combined with Neural Flossing Technique (NFT) in individuals with lumbar radiculopathy. A total of 22 participants aged 25-55 will be recruited through non-probability convenience sampling from rehabilitation clinics in Lahore and randomly assigned to two intervention groups

Trial Health

75
On Track

Trial Health Score

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

Enrollment
22

participants targeted

Target at below P25 for not_applicable

Timeline
3mo left

Started Jul 2025

Geographic Reach
1 country

1 active site

Status
active not recruiting

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 Progress81%
Jul 2025Sep 2026

Study Start

First participant enrolled

July 6, 2025

Completed
11 months until next milestone

First Submitted

Initial submission to the registry

June 1, 2026

Completed
4 days until next milestone

First Posted

Study publicly available on registry

June 5, 2026

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 5, 2026

Expected
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

September 6, 2026

Last Updated

June 5, 2026

Status Verified

June 1, 2026

Enrollment Period

1.1 years

First QC Date

June 1, 2026

Last Update Submit

June 4, 2026

Conditions

Keywords

flexibilitylumbar radiculopathymyokinetic stretchingneural flossingpainmobility

Outcome Measures

Primary Outcomes (5)

  • Numeric Pain Rating Scale (NPRS)

    The Numeric Pain Rating Scale (NPRS) measures a patient's self-reported pain intensity on a scale from 0 to 10. A score of 0 indicates no pain, 1-3 is mild, 4-6 is moderate, and 7-10 represents severe pain.

    baseline to 4 week

  • Oswestry Disability Index (ODI)

    The Oswestry Disability Index (ODI) is used to assess the impact of low back pain on a patient'sADLs. It includes 10 sections, 0 to 5each, with the total score expressed as a percentage. The results categorize disability from minimal (0-20%) to bed-bound or exaggerated symptoms (81-100%), helping quantify the degree of functional limitation

    baseline to 4 week

  • Sit and Reach Test

    The Sit and Reach Test is used to assess the flexibility of the hamstrings and lower back. The patient sits with legs extended and reaches forward along a marked measuring line. Scores above 10 cm indicate excellent flexibility, 0-10 cm is average, and negative values suggest poor flexibility, often linked to hamstring tightness or lumbar dysfunction.

    baseline to 4 week

  • Muscle Strength Assessment: Functional Trunk Strength Tests

    Functional Trunk Strength Tests assess the strength and endurance of lumbar flexors and extensors through movements like sit-ups or back extensions. The patient performs prone chest raises. Greater repetitions or longer hold times indicate better trunk strength and endurance, while early fatigue suggests weakness.

    baseline to 4 week

  • Modified Schober Test

    The Modified Schober Test assesses lumbar spine flexibility during forward bending by measuring the increase in distance between marked points on the lower back. An increase of ≥5 cm indicates normal lumbar mobility, while \<5 cm suggests restricted flexion.

    baseline to 4 week

Study Arms (2)

conventional

EXPERIMENTAL

heating pad and Range of motion

Other: Myokinetic stretchingOther: nyokinetic stretching with neural flossing technique

conventional therapy

ACTIVE COMPARATOR

heating pad and range of motion exercises

Other: Myokinetic stretchingOther: nyokinetic stretching with neural flossing technique

Interventions

* Light aerobic activity (e.g., stationary cycling or brisk walking) to increase blood flow and prepare muscles for stretching• Myokinetic Stretching Technique (MST): - Target muscles: hamstrings, lumbar paraspinals, gluteals, hip flexors. - Involves both active (patient-initiated) and passive (therapist-assisted) stretches. * Sustained stretches held for 20-30 seconds with 3-5 repetitions. * Focus on length-tension balance, postural correction, and neuromuscular re- education. Progressive loading as tolerated

conventionalconventional therapy

* Myokinetic stretching with Neural Flossing Technique (NFT): - * Target: sciatic nerve and related neural structures. - * Performed as oscillatory, controlled gliding movements ("sliders" and "tensioners"). * Techniques include supine straight leg raise with ankle dorsiflexion and cervical flexion/extension. - 3 sets of 10-15 repetitions, increasing intensity and duration based on tolerance. Aims to reduce neural tension and improve neurodynamic mobility.

conventionalconventional therapy

Eligibility Criteria

Age30 Years - 50 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Clinically pre diagnosed lumbar radiculopathy
  • Radiating low back pain persisting for \>3 weeks
  • Positive Straight Leg Raise Test (SLR) or Slump Test

You may not qualify if:

  • Pregnancy , Inflammatory or autoimmune spinal diseases
  • Severe neurological deficits
  • Inability to participate in active exercises or follow instructions

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Unknown Facility

Lahore, Punjab Province, 54000, Pakistan

Location

MeSH Terms

Conditions

RadiculopathyPain

Condition Hierarchy (Ancestors)

Peripheral Nervous System DiseasesNeuromuscular DiseasesNervous System DiseasesNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Anam Iqbal, DPT

    Riphah International University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

June 1, 2026

First Posted

June 5, 2026

Study Start

July 6, 2025

Primary Completion (Estimated)

August 5, 2026

Study Completion (Estimated)

September 6, 2026

Last Updated

June 5, 2026

Record last verified: 2026-06

Data Sharing

IPD Sharing
Will not share

Locations