- ICH GCP
- US-Register für klinische Studien
- Klinische Studie 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
Studienübersicht
Status
Bedingungen
Detaillierte Beschreibung
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.
Studientyp
Einschreibung (Tatsächlich)
Phase
- Unzutreffend
Kontakte und Standorte
Studienorte
-
-
-
Giza, Ägypten
- Cairo University
-
-
Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
- Erwachsene
Akzeptiert gesunde Freiwillige
Beschreibung
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.
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Behandlung
- Zuteilung: Zufällig
- Interventionsmodell: Parallele Zuordnung
- Maskierung: Single
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
|
Experimental: 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.
|
19 subjects received combined dry cupping therapy, Muscle energy technique, and conventional physical therapy for eight weeks.
|
|
Experimental: Group B (Cupping group)
Group B (Cupping group): This group of nineteen subjects received dry cupping therapy and conventional physical therapy.
|
19 subjects received combined dry cupping therapy and conventional physical therapy for eight weeks.
|
|
Experimental: Group C (MET group)
Group C (MET group): This group of nineteen subjects received Muscle energy techniques and conventional physical therapy.
|
19 subjects received combined Muscle energy technique, and conventional physical therapy for eight weeks.
|
|
Aktiver Komparator: Group D (Control group)
Group D (Control group): This group of nineteen subjects received conventional physical therapy alone
|
19 subjects received only conventional physical therapy for eight weeks.
|
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Neck Disability Index (NDI)
Zeitfenster: At baseline and re assessed following 8 weeks
|
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.
|
At baseline and re assessed following 8 weeks
|
|
craniovertebral angle (CVA)
Zeitfenster: At baseline and re assessed following 8 weeks
|
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.
|
At baseline and re assessed following 8 weeks
|
|
Sagittal Shoulder-C7 Angle (SSA)
Zeitfenster: At baseline and re assessed following 8 weeks
|
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.
|
At baseline and re assessed following 8 weeks
|
Mitarbeiter und Ermittler
Sponsor
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn (Tatsächlich)
Primärer Abschluss (Geschätzt)
Studienabschluss (Geschätzt)
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Tatsächlich)
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Zusätzliche relevante MeSH-Bedingungen
Andere Studien-ID-Nummern
- 012/006489
Arzneimittel- und Geräteinformationen, Studienunterlagen
Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt
Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .
Klinische Studien zur Upper-Crossed-Syndrom
-
Riphah International UniversityRekrutierung
-
Riphah International UniversityAbgeschlossenUpper-Crossed-SyndromPakistan
-
Riphah International UniversityNoch keine RekrutierungUpper-Crossed-SyndromPakistan
-
Riphah International UniversityNoch keine RekrutierungUpper-Crossed-SyndromPakistan
-
Cairo UniversityNoch keine RekrutierungUpper-Crossed-Syndrom
-
China Medical University HospitalRekrutierung
-
Riphah International UniversityRekrutierungNur Kinder | Upper-Crossed-SyndromPakistan
-
Universiti Putra MalaysiaAbgeschlossen
-
Cairo UniversityNoch keine Rekrutierung
-
Foundation University IslamabadAbgeschlossen
Klinische Studien zur combined therapy teatment
-
Sahmyook UniversityAbgeschlossenSchmerzen im unteren RückenKorea, Republik von
-
CooperVision International Limited (CVIL)AbgeschlossenKurzsichtigkeitVereinigte Staaten
-
Rong WenchaoAbgeschlossenKörperliche AbhängigkeitChina
-
Bahçeşehir UniversityAbgeschlossenSportverletzungTruthahn
-
Karadeniz Technical UniversityAnmeldung auf Einladung
-
Children's Hospital Medical Center, CincinnatiAbgeschlossenIntraventrikuläre BlutungVereinigte Staaten
-
Columbia UniversityBeendet
-
Atatürk Chest Diseases and Chest Surgery Training...AbgeschlossenSchmerzen, postoperativ | Block der vorderen Serratus-Ebene | Thoraxchirurgie, videoassistiert | Multimodale AnalgesieTruthahn
-
Yuzuncu Yil UniversityRekrutierungFrühgeborene | Schlafqualität | Vitalfunktionen | NICU | İnfant Stress | SäuglingskomfortTürkei (türkiye)
-
Hospital Clinic of BarcelonaRekrutierung