- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT07628426
Effects of Myokinetic Stretching Technique With And Without Neural Flossing Technique In Lumbar Radiculopathy
4. juni 2026 opdateret af: Riphah International University
Effects of Myokinetic Stretching Technique With And Without Neural Flossing Technique On Pain, Flexibility, And Mobility In Patients With Lumbar Radiculopathy
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
Studieoversigt
Status
Aktiv, ikke rekrutterende
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
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.
Both groups will receive treatment thrice weekly for six weeks.
Outcome measures include pain intensity (NPRS), functional disability (ODI), flexibility (Sit and Reach Test, Modified Schober Test), and trunk strength (Functional Trunk Strength Tests).
Data will be analyzed using SPSS v24, with appropriate statistical tests applied based on data distribution.
Undersøgelsestype
Interventionel
Tilmelding (Anslået)
22
Fase
- Ikke anvendelig
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
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Punjab Province
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Lahore, Punjab Province, Pakistan, 54000
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-
Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
Tager imod sunde frivillige
Ingen
Beskrivelse
Inclusion Criteria:• Age between 30-50 years
- Clinically pre diagnosed lumbar radiculopathy
- Radiating low back pain persisting for >3 weeks
- Positive Straight Leg Raise Test (SLR) or Slump Test
- LDI or Oswestry Disability Index <50% Exclusion Criteria:• Recent spinal surgery or acute spinal trauma
- Pregnancy , Inflammatory or autoimmune spinal diseases
- Severe neurological deficits
- Inability to participate in active exercises or follow instructions
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Enkelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
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Eksperimentel: conventional
heating pad and Range of motion
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Aktiv komparator: conventional therapy
heating pad and range of motion exercises
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Numeric Pain Rating Scale (NPRS)
Tidsramme: baseline to 4 week
|
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)
Tidsramme: baseline to 4 week
|
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
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baseline to 4 week
|
|
Sit and Reach Test
Tidsramme: baseline to 4 week
|
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.
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baseline to 4 week
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Muscle Strength Assessment: Functional Trunk Strength Tests
Tidsramme: baseline to 4 week
|
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.
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baseline to 4 week
|
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Modified Schober Test
Tidsramme: baseline to 4 week
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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
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Efterforskere
- Ledende efterforsker: Anam Iqbal, DPT, Riphah International University
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart (Faktiske)
6. juli 2025
Primær færdiggørelse (Anslået)
5. august 2026
Studieafslutning (Anslået)
6. september 2026
Datoer for studieregistrering
Først indsendt
1. juni 2026
Først indsendt, der opfyldte QC-kriterier
4. juni 2026
Først opslået (Faktiske)
5. juni 2026
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
5. juni 2026
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
4. juni 2026
Sidst verificeret
1. juni 2026
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- REC/RCR&AHS/25/0208
Plan for individuelle deltagerdata (IPD)
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