- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT05730426
Comparison Between Deep Dry Needling and Muscle Energy Technique on Chronic Non-specific Neck Pain Patients.
Deep Dry Needling Versus Muscle Energy Technique on Chronic Non-specific Neck Pain; a Randomized Controlled Trial.
Studieoversigt
Status
Betingelser
Intervention / Behandling
Undersøgelsestype
Tilmelding (Faktiske)
Fase
- Ikke anvendelig
Kontakter og lokationer
Studiesteder
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Mansoura, Egypten
- Delta University for science and technology.
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Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
Inclusion Criteria:
- Age 18 and 40 years.
- Current neck pain.
- Presence of at least one or two trigger points .
- Patients are diagnosed and referred from orthopedist complaining from chronic neck pain for at least 12 weeks.
- No clinical treatment for neck pain within the past month.
- lacked a history of neck and shoulder myopathy, neuropathy, myelopathy and neck, torso and shoulder surgery.
- Patients with body mass index less than 30 kg/m2.
Exclusion Criteria:
- Patients outside the target range.
- Neck pain associated with vertigo.
- Osteoporosis.
- Diagnosed psychological disorders.
- Fibromyalgia syndrome.
- Vertebral fractures.
- Spinal stenosis.
- Tumors.
- Previous neck surgery.
- Red flags (night pain, severe muscle spasm, loss of involuntary weight, symptom mismatch).
- Physiotherapeutic treatment continued in the last 3 months. Any contraindications for deep dry needling such as anticoagulants, infections and bleeding.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Dobbelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
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Aktiv komparator: Group A
In addition to Transcutaneous Electrical Nerve Stimulation (TENS) (typical,100 Hz, 20 mins), Infrared (7 mins), and Exercises (Cervical Stability Exercises through activation of deep neck flexors), patients received deep dry needling on active trigger points in selected muscles (upper trapezius, levator scapulae, and sternocleidomastoid ), 3 sessions/week, for 4 weeks period.
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Method to decrease pain and improve function in musculoskeletal disorders.
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Aktiv komparator: Group B
In addition to Transcutaneous Electrical Nerve Stimulation (TENS) (typical,100 Hz, 20 mins), Infrared (7 mins), and Exercises (Cervical Stability Exercises through activation of deep neck flexors), patients received muscle energy technique (post isometric relaxation) in selected muscles (upper trapezius, levator scapulae, and sternocleidomastoid ), 3 sessions/week, for 4 weeks period.
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Method to decrease pain and improve function in musculoskeletal disorders.
Andre navne:
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Placebo komparator: Group C
Patients receive Transcutaneous Electrical Nerve Stimulation (TENS) (typical,100 Hz, 20 mins), Infrared (7 mins), and Exercises (Cervical Stability Exercises through activation of deep neck flexors) , 3 sessions/week, for 4 weeks period.
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Method to decrease pain and improve function in musculoskeletal disorders.
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
---|---|---|
Change in pain intensity from baseline to 4 weeks after.
Tidsramme: ved baseline og efter 4 uger fra baseline.
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Visuel analog skala (VAS)
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ved baseline og efter 4 uger fra baseline.
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Change in function from baseline to 4 weeks after.
Tidsramme: at baseline and after 4 weeks from the baseline.
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The Neck Disability Index (NDI) The NDI questionnaire (scored out of 50) was used to measure the patient's perceived disability resulting from their neck pain. The score for each section was from 0 to 5, with 0 represented the highest level of function and 5 represented the lowest level of function. Total NDI scores were shown as a percentage. A high score corresponded to a higher degree of disability.
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at baseline and after 4 weeks from the baseline.
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Change in cervical range of motion (ROM) in sagittal, coronal and transverse planes from baseline to 4 weeks after.
Tidsramme: at baseline and after 4 weeks from the baseline.
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AcuAngle® Inclinometer: (Baseline® AcuAngle Inclinometer; Elmsford, NY, U.S. PAT 2194335, 2-D Functions)
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at baseline and after 4 weeks from the baseline.
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Change in pain threshold from baseline to 4 weeks after.
Tidsramme: at baseline and after 4 weeks from the baseline.
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Pain Pressure Algometer: (BASELINE 22-POUND DOLORIMETER).
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at baseline and after 4 weeks from the baseline.
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Samarbejdspartnere og efterforskere
Sponsor
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Primær færdiggørelse (Faktiske)
Studieafslutning (Faktiske)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- P.T.REC/012/003913
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
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