- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT07654543
Dry Cupping Therapy and Muscle Energy Technique on Upper Crossed Syndrome
Effect of Combined Dry Cupping Therapy and Muscle Energy Technique on Upper Crossed Syndrome Patients. A Randomized Control Study
Studieoversigt
Status
Betingelser
Detaljeret beskrivelse
This study evaluated and compared the therapeutic efficacy of combining Dry Cupping therapy with the Muscle Energy Technique (MET) against each intervention applied independently, focusing on three core parameters: Neck Disability Index (NDI), Craniovertebral Angle (CVA), and Sagittal Shoulder-C7 Angle (SSA).
Methods: A pre-test post-test double-blinded randomized controlled trial design was employed. Seventy-six adults (aged 20-40 years) diagnosed with UCS were randomly allocated into four equal experimental groups (n = 19 per group): Group A received combined dry cupping and MET with conventional therapy; Group B received dry cupping with conventional therapy; Group C received MET with conventional therapy; and Group D received conventional therapy alone. Interventions were conducted over an 8-week period. Primary outcomes included functional impairment via the Arabic version of the NDI, and objective sagittal alignment parameters (CVA and SSA) measured using precision photometry via the Kinovea software application.
Undersøgelsestype
Tilmelding (Faktiske)
Fase
- Ikke anvendelig
Kontakter og lokationer
Studiesteder
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Giza, Egypten
- Cairo University
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Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
Tager imod sunde frivillige
Beskrivelse
Inclusion Criteria:
- Participant inclusion was restricted to individuals between 20 and 40 years of age.
- The exact diagnostic criteria required a baseline craniovertebral angle (CVA) of less than 48 degrees.
- a sagittal shoulder-C7 angle (SSA) of less than 52 degrees.
Exclusion Criteria:
- acute post-surgical conditions
- structural spinal deformities (e.g., severe fixed structural scoliosis)
- cervical radiculopathy, or localized dermal infections contradicting cupping application.
Studieplan
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: Group A (Combined group)
Group A (Combined group): This group of nineteen subjects received combined dry cupping therapy, Muscle energy techniques, and conventional physical therapy.
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19 subjects received combined dry cupping therapy, Muscle energy technique, and conventional physical therapy for eight weeks.
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Eksperimentel: Group B (Cupping group)
Group B (Cupping group): This group of nineteen subjects received dry cupping therapy and conventional physical therapy.
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19 subjects received combined dry cupping therapy and conventional physical therapy for eight weeks.
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Eksperimentel: Group C (MET group)
Group C (MET group): This group of nineteen subjects received Muscle energy techniques and conventional physical therapy.
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19 subjects received combined Muscle energy technique, and conventional physical therapy for eight weeks.
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Aktiv komparator: Group D (Control group)
Group D (Control group): This group of nineteen subjects received conventional physical therapy alone
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19 subjects received only conventional physical therapy for eight weeks.
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Neck Disability Index (NDI)
Tidsramme: At baseline and re assessed following 8 weeks
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Perceived functional limitations resulting from regional impairment were measured using the validated Arabic version of the NDI questionnaire.
This instrument evaluates 10 clinical sections (including activities of daily living, concentration, and pain profiles) scored from 0 to 5 per item, yielding a cumulative score out of 50.
Higher aggregate indices represent greater functional disability.
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At baseline and re assessed following 8 weeks
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craniovertebral angle (CVA)
Tidsramme: At baseline and re assessed following 8 weeks
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This biomechanical index reflects the architectural severity of forward head posture.
It is defined as the angle formed between a horizontal line drawn through the spinous process of C7 and an intersecting line extending from the tragus of the ear to the C7 landmark.
CVA was measured using precision digital photogrammetry via the Kinovea software application.
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At baseline and re assessed following 8 weeks
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Sagittal Shoulder-C7 Angle (SSA)
Tidsramme: At baseline and re assessed following 8 weeks
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This geometric marker quantifies shoulder roundedness and anterior protraction.
It is formed by the intersection of a horizontal reference line passing through the lateral aspect of the acromion with a line drawn from the C7 spinous process to the lateral acromion.
SSA was measured using precision digital photogrammetry via the Kinovea software application.
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At baseline and re assessed following 8 weeks
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Samarbejdspartnere og efterforskere
Sponsor
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Primær færdiggørelse (Anslået)
Studieafslutning (Anslået)
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
- 012/006489
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
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