- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT05258201
Effect of Muscle Energy Technique Versus Strain-counterstrain on Upper Trapezius Trigger Points
21. april 2022 opdateret af: Riphah International University
Effect of Muscle Energy Technique Versus Strain-Counterstrain on Upper Trapezius Myofascial Active Trigger Points. A Randomized Control Trial
Aim of the study To determine the comparative effects of muscle energy technique and strain counter strain in upper trapezius trigger point.
Studieoversigt
Status
Afsluttet
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
A Randomized Controlled trial will be conducted after approval of synopsis.
To enroll patients Purposive sampling technique will be used.
Patients will be selected according to the pre-defined inclusion and exclusion criteria.
The enrolled patients will be allocated into two groups, group A and group B. On Group A muscle energy technique will be applied for 30 seconds and repeat 3 to 5 times per on treatment session and Group B will be treated with strain counter strain for 20-30 seconds and repeat this process for up to five times.
Assessment will be done at baseline, 2nd week, 4th week and 6th week of treatment.
Follow up will be assessed 15 days after completion of treatment protocol.
The patients' outcome will be measured by Visual Analog Scale for pain intensity and Neck Disability Index .
Informed consent will be taken from each patient.
Statistical Package of Social Sciences software, version 20 will be used for the analysis of data.
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
50
Fase
- Ikke anvendelig
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
-
-
Punjab
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Faisalabad, Punjab, Pakistan, 38000
- Ripah International University
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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
18 år til 34 år (Voksen)
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Alle
Beskrivelse
Inclusion Criteria:
- Participants who are 18 to 34 years old
- In upper trapezius From 2 weeks Had mechanical neck pain and was diagnosed with active myofacial Trigger points
- Subjects have to exhibit a tendor point in the upper trapezius muscle either on the left or right side
- Local pain is greater than 3/10 on Visual Analog scale
Exclusion Criteria:
- Patient with cervical radiculopathy
- Patients with Fibromyalgia syndrome
- Patients who had cervical spine surgery
- Patient with myelopathy
- Patients who had myofacial pain therapy
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 |
---|---|
Eksperimentel: Muscle Energy Technique
Muscle energy Technique will be applied on the subjects, when they will be lying supine and on the effect side therapist will stabilize shoulder by one hand, while the ear / mastoid area of the affected side will be hold by opposite hand.
The head and neck will be bend to contralateral side, then bends on the same side.
Subject will raise his shoulder with the shoulder fixed to the ear with less effort than the maximum.
Isometric contraction will be maintain for 7-10 seconds.
This position will be held for 30 seconds and repeat three to five times per on treatment session
|
Muscle Energy Technique is a common way to achieve muscle tension release (stop) before stretching other's adductor muscles
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Eksperimentel: Strain-counterstrain
Strain And Counter Strain will be applied on subject in normal position and will be produced by placing the muscle in a short / relaxed position, the point where the pain will reduce of at least 70% will be produce will easily define.
The patient will be in a supine position while the doctor will place the labial arm in flexion, abduction and external rotation to reduce the reported Trp pain.
Once the position is easy to find, the pressure will be apply to the Trp and will be hold for 20-30 seconds and repeat this process for up to five times
|
Strain-counterstrain is also used for manual Trigger Point processing.
This involves identifying active TRP and then applying pressure until a ridiculous reaction occurs.
The area is then positioned to reduce tension in the injured muscle and later reduce tripod pain.
When the pain subsides, the tissues that are most stressed feel relaxed and there is a local decrease in the ground
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
---|---|---|
Visuel analog skala
Tidsramme: 12. uge
|
En visuel analog skala er et måleinstrument, der forsøger at måle en karakteristik eller holdning, der menes at spænde over et kontinuum af værdier og ikke let kan måles direkte.
Det bruges ofte i epidemiologisk og klinisk forskning til at måle intensiteten eller hyppigheden af forskellige symptomer.
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12. uge
|
Neck Disability Index
Tidsramme: 12th Week
|
The Neck Disability Index is a 10-item questionnaire that measures a patient's self-reported neck pain related disability.
A higher Neck Disability Index score means the greater a patient's perceived disability due to neck pain
|
12th Week
|
Goniometer
Tidsramme: 12th Week
|
Goniometer has been the most widely used tool for measuring joint range of motion.
To ensure reliable measurement, standardized, specific positions and landmarks are used to measure Cervical lateral flexion range of motion.
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12th Week
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Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
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)
1. marts 2021
Primær færdiggørelse (Faktiske)
20. marts 2022
Studieafslutning (Faktiske)
25. marts 2022
Datoer for studieregistrering
Først indsendt
20. februar 2022
Først indsendt, der opfyldte QC-kriterier
20. februar 2022
Først opslået (Faktiske)
28. februar 2022
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
22. april 2022
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
21. april 2022
Sidst verificeret
1. april 2022
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- REC-FSD-00268
Plan for individuelle deltagerdata (IPD)
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