Spray and Stretch Technique Versus Strain Counter Strain in Patients With Non Specific Low Back Pain
27 luglio 2026 aggiornato da: Riphah International University
Comparative Effect of Spray and Stretch Technique Versus Strain Counter Strain on Hamstring Muscles for Pain , Disability and Mobility in Patients With Non Specific Low Back Pain
Non-specific low back pain refers to pain in the lower back region that cannot be attributed to a specific identifiable pathology such as infection, tumor, osteoporosis, lumbar disc herniation, spinal stenosis or fracture.
It is the most common type of low back pain, accounting for about 85-90% of cases.
Non specific low back pain is posteriorly occurring that is located between lower rib margin and gluteal fold.
It is exacerbated by sustained back postures, back movements or back muscle imbalances.
The aim of study is to find out which technique whether Spray and stretch technique or strain Counter strain works better in reducing pain ,improving movement ,and decreasing disability caused by tight hamstring muscles in people with non specific low Back Pain.
Panoramica dello studio
Stato
Reclutamento
Condizioni
Descrizione dettagliata
This double blinded randomized Clinical Trial will be conducted at Ibne Siena Hospital MULTAN through consecutive sampling technique on 30 patients which will be allocated using simple random sampling through sealed opaque enveloped into Group A and Group B. Group A will be treated with spray and stretch technique and Group B will be treated with strain counter technique at the frequency of 2 sets with 5 repetitions and thrice a week.
Outcome measures will be conducted through NPRS, ODI, AKE ,PKET and SLR before treatment and after 4 weeks.
Data will be analyzed during SPSS software version 26.
After assessing normality of data by Shapiro-wilk test, it will be decided either parametric or non parametric test will be used within a group or between two groups.
Tipo di studio
Interventistico
Iscrizione (Stimato)
30
Fase
- Non applicabile
Contatti e Sedi
Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.
Contatto studio
- Nome: Samrood Akram, PhD*
- Numero di telefono: 03324806143
- Email: samrood.akram@riphah.edu.pk
Backup dei contatti dello studio
- Nome: Amna Zia, PhD*
- Numero di telefono: 03244686993
- Email: amna.zia@kemu.edu.pk
Luoghi di studio
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Punjab Province
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Multan, Punjab Province, Pakistan
- Reclutamento
- Ibne sina hospital and research institute.
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Contatto:
- Sajad Rasheed, MS-OMPT
- Numero di telefono: 0300 6309825
- Email: sajidch71@hotmail.com
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Criteri di partecipazione
I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.
Criteri di ammissibilità
Età idonea allo studio
- Adulto
Accetta volontari sani
No
Descrizione
Inclusion Criteria:
AGE(35 to 50)
- Gender (both male and female)
- Negative lasegue test
- Negative slump test
- Negative prone instability test
Exclusion Criteria:
Fracture or instability (4)
- History of cancer
- Inflammatory condition like ankylosing spondylitis
- Neurological deficits like cauda equina syndrome or motor weakness
- History of previous of previous lumber surgery
- Pregnancy
- Structural deformity like scoliosis
- Herniated disc
- Nerve compression
- Spinal stenosis
Piano di studio
Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: Randomizzato
- Modello interventistico: Assegnazione parallela
- Mascheramento: Separare
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
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Sperimentale: Spray and stretch technique on Hamstrings muscle
The spray and stretch technique is a physical therapy method used to inactivate myofascial trigger points, reduce muscle spasms, and increase range of motion.
It works by applying a vapocoolant spray to numb the skin, which interrupts the pain signal, allowing the therapist to safely stretch the muscle
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The participant will be positioned in a comfortable supine lying position on a treatment table in a quiet and suitable clinical environment. Before starting the intervention, the procedure will be explained to the participant in simple language, and verbal confirmation of comfort will be obtained. The affected lower limb will be exposed appropriately while ensuring privacy, modesty, and warmth through proper draping with towels or sheets. The participant will be instructed to relax the lower limb during the procedure. The hip will be maintained in a neutral position, and the knee will be kept straight or slightly flexed according to the participant's comfort before the stretching component begins. The therapist will first inspect the posterior thigh region to ensure that the skin is intact and suitable for vapocoolant application. The presence of any open wound, skin infection, rash, hypersens |
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Comparatore attivo: Strain and counter strain technique on Hamstring muscle
Strain-Counterstrain (SCS) is a gentle, hands-on physical therapy technique used to relieve low back pain by "resetting" the nervous system.
By placing the body in specific, pain-free positions, it relaxes tight muscles, reduces muscle guarding, and improves mobility
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identify the tender point Palpate the hamstring while the patient is prone or side lying locate the most tender point in belly of the muscle or near the ischial tuberosity Establish a pain scale and Ask the patient to rate the tenderness from 0 to 10 (10 being the most painful).Position of ease will be achieved by Flexing the patient's knee to about 70 to 90 degrees .Slightly abduct and externally rotate the leg to shorten the hamstring muscle (the position may vary depending on the muscle .The goal is to reduce tenderness by at least 70% .Hold the position and Maintain this position of comfort for 90 seconds Encourage the patient to relax during this time .Return the leg passively to a neutral position to avoid reactivating the trigger point .Palpate the tender point again and ask for a new pain rating.
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Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
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Numeric pain rate scale (NPRS)
Lasso di tempo: Baseline and after 4 weeks of intervention
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Pain intensity will be assessed using the 11-point Numeric Pain Rating Scale.
Participants will rate their current low back pain from 0 to 10, where 0 indicates "no pain" and 10 indicates the "worst imaginable pain."
The score will be recorded in points, with higher scores indicating greater pain intensity.
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Baseline and after 4 weeks of intervention
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Active knee extension
Lasso di tempo: Baseline and after 4 weeks of intervention
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Hamstring flexibility will be assessed using the Active Knee Extension Test.
The participant will lie in the supine position with the hip flexed to 90 degrees and will actively extend the knee as far as possible while maintaining the hip position.
The knee extension angle will be measured in degrees using a goniometer.
A smaller knee-flexion deficit indicates greater hamstring flexibility.Positive AKE (For males, a positive knee extension angle is >33.0°,
whereas for females, it is >24)
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Baseline and after 4 weeks of intervention
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Passive knee extension test (PKET)
Lasso di tempo: Baseline and after 4 weeks
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Hamstring flexibility will be assessed using the Passive Knee Extension Test.
With the participant in the supine position and the hip maintained at 90 degrees of flexion, the examiner will passively extend the knee until resistance or discomfort is reached.
The knee extension angle will be measured in degrees using a goniometer.
A greater knee-extension angle indicates greater hamstring flexibility.
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Baseline and after 4 weeks
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Oswestry Disability Index
Lasso di tempo: Baseline and after 4 weeks
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Low back pain-related disability will be assessed using the Oswestry Disability Index.
The questionnaire contains 10 sections, with each section scored from 0 to 5. The total score will be converted into a percentage ranging from 0% to 100%, where higher scores indicate greater disability.
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Baseline and after 4 weeks
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Straight leg raise
Lasso di tempo: Baseline and after 4 weeks
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Straight leg raise range of motion will be assessed with the participant in the supine position.
The examiner will passively raise the participant's lower limb while maintaining the knee in extension until resistance or discomfort is reported.
The hip-flexion angle will be measured in degrees using a goniometer.
A greater angle indicates greater posterior-chain flexibility and straight leg raise range of motion.
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Baseline and after 4 weeks
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Collaboratori e investigatori
Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.
Sponsor
Investigatori
- Investigatore principale: Amna Zia, PhD*, Riphah International University, Lahore
- Investigatore principale: Zaib un Nisa, Riphah International University, Lahore
Pubblicazioni e link utili
La persona responsabile dell'inserimento delle informazioni sullo studio fornisce volontariamente queste pubblicazioni. Questi possono riguardare qualsiasi cosa relativa allo studio.
Pubblicazioni generali
- Shipton EA. Physical Therapy Approaches in the Treatment of Low Back Pain. Pain Ther. 2018 Dec;7(2):127-137. doi: 10.1007/s40122-018-0105-x. Epub 2018 Sep 18.
- Koura G, Hamada H, Mohamed YE, Balbaa AA, El-Nassag BA, Baghdadi ARJHM. Impact of strain-counterstrain on treatment of acute nonspecific low back pain: a single-blind randomized controlled trial. 2020;22(1):42-9.
- Seif HE, Alenazi A, Hassan SM, Kachanathu SJ, Hafez ARJOJoT, Rehabilitation. The effect of stretching hamstring, gastrocnemius, iliopsoas and back muscles on pain and functional activities in patients with chronic low back pain: a randomized clinical trial. 2015;3(4):139-45.
- Gou Y, Lei H, Chen X, Wang X. The effects of hamstring stretching exercises on pain intensity and function in low back pain patients: A systematic review with meta-analysis of randomized controlled trials. SAGE Open Med. 2024 Jul 29;12:20503121241252251. doi: 10.1177/20503121241252251. eCollection 2024.
- Haile G, Hailemariam TT, Haile TG. Effectiveness of Ultrasound Therapy on the Management of Chronic Non-Specific Low Back Pain: A Systematic Review. J Pain Res. 2021 May 17;14:1251-1257. doi: 10.2147/JPR.S277574. eCollection 2021.
- Riaz SA, Usman MJPJoR. Effect of Static Stretching of Hamstring on Non-Specific Low Back Pain. 2023;12(1):43-51.
- Dobija L, Pereira B, Cohen-Aknine G, Roren A, Dupeyron A, Coudeyre E. Immediate effect of passive hamstring stretching on flexibility and relationship with psychosocial factors in people with chronic low back pain. Heliyon. 2023 Sep 4;9(9):e19753. doi: 10.1016/j.heliyon.2023.e19753. eCollection 2023 Sep.
- Ahmed J, Anwar K, Sajjad AGJRJoHS. Effects of strain counter strain technique in treatment of chronic mechanical low back pain: a randomized controlled trail. 2021;3(2):85-91
- Hariharasudhan R, Balamurugan JJSjosm. A randomized double-blinded study of effectiveness of strain counter-strain technique and muscle energy technique in reducing pain and disability in subjects with mechanical low back pain. 2014;14(2):83-8.
- Ellythy MAJBFPT. Efficacy of muscle energy technique versus strain counter strain on low back dysfunction. 2012;17(2):29-35.
Studiare le date dei record
Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.
Studia le date principali
Inizio studio (Effettivo)
20 giugno 2026
Completamento primario (Stimato)
20 agosto 2026
Completamento dello studio (Stimato)
20 settembre 2026
Date di iscrizione allo studio
Primo inviato
21 luglio 2026
Primo inviato che soddisfa i criteri di controllo qualità
27 luglio 2026
Primo Inserito (Effettivo)
28 luglio 2026
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
28 luglio 2026
Ultimo aggiornamento inviato che soddisfa i criteri QC
27 luglio 2026
Ultimo verificato
1 luglio 2026
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Termini MeSH pertinenti aggiuntivi
Altri numeri di identificazione dello studio
- REC/RCR & AHS/25/0135 Nisa
Piano per i dati dei singoli partecipanti (IPD)
Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?
NO
Informazioni su farmaci e dispositivi, documenti di studio
Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti
No
Studia un dispositivo regolamentato dalla FDA degli Stati Uniti
No
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .