beta
Trial Radar IA
Lo studio clinico NCT06407817 per Capsulite adesiva è in arruolamento. Consulti la vista a schede del Radar degli Studi Clinici e gli strumenti di scoperta IA per tutti i dettagli. Oppure, ponga pure una domanda qui.
Un studio corrisponde ai criteri del filtro
Vista a schede
Torna alla ricerca

Comparative Effects Of Spencer and Reverse Distraction Technique In Patients With Adhesive Capsulitis 50

In arruolamento
I dettagli dello studio clinico sono disponibili principalmente in inglese. Tuttavia, Trial Radar IA può essere d'aiuto! Basta cliccare su 'Spiega lo studio' per visualizzare e discutere le informazioni sullo studio nella lingua selezionata.
La sperimentazione clinica NCT06407817 è uno studio interventistico per Capsulite adesiva, attualmente in arruolamento. Avviato il 1 febbraio 2024, prevede di arruolare 50 partecipanti. Sotto la guida di l'Università internazionale Riphah, dovrebbe concludersi entro il 1 gennaio 2025. I dati più recenti da ClinicalTrials.gov sono stati aggiornati l'ultima volta il 27 dicembre 2024.
Sommario breve
To compare the effects of spencer and reverse distraction technique in patients with adhesive capsulitis
Descrizione dettagliata
Adhesive capsulitis, also known as frozen shoulder, is an inflammatory condition characterized by shoulder stiffness, pain, and significant loss of passive range of motion. Adhesive capsulitis has a prevalence of approximately 2% to 5% in the general population, with a mean onset of age of 55.

A randomized clinical trial will be conducted at Ibne Sina Hospital, Multan . Non probability convenience sampling technique...

Mostra di più
Titolo ufficiale

Comparative Effects Of Spencer and Reverse Distraction Technique In Patients With Adhesive Capsulitis

Patologie
Capsulite adesiva
Altri ID dello studio
  • REC/RCR&AHS/23/0184
Numero NCT
NCT06407817
Data di inizio (effettiva)
2024-02-01
Ultimo aggiornamento pubblicato
2024-12-27
Data di completamento (stimata)
2025-01
Arruolamento (previsto)
50
Tipo di studio
Interventistico
FASE
N.D.
Stato
In arruolamento
Scopo principale
Trattamento
Allocazione
Randomizzato
Modello di intervento
In parallelo
Mascheramento
Singolo
Bracci / Interventi
Gruppo/Braccio di partecipantiIntervento/Trattamento
SperimentaleSpencer's technique
This group will receive the Spencer's technique.
Spencer technique
No of repetitions; 3 sets for 10 repetitions with 1 minute rest between sets No Of Sessions Per Week: 3 Per Weeks for 6 weeks (40 Min per Session)
reverse distraction technique
No of repetitions; 10 ( Shoulder Abduction)10 ( Shoulder Flexion) 10 (Shoulder External Rotation) No Of Sessions Per Week: 3 Per Weeks for 6 weeks (40 Min Per Session)
Comparatore attivoreverse distraction technique
This group will recieve reverse distraction technique
Spencer technique
No of repetitions; 3 sets for 10 repetitions with 1 minute rest between sets No Of Sessions Per Week: 3 Per Weeks for 6 weeks (40 Min per Session)
reverse distraction technique
No of repetitions; 10 ( Shoulder Abduction)10 ( Shoulder Flexion) 10 (Shoulder External Rotation) No Of Sessions Per Week: 3 Per Weeks for 6 weeks (40 Min Per Session)
Esito primario
Misure di esitoDescrizione della misuraArco temporale
pain : numerical pain rating scale
Patients' overall assessment of pain will be provided using the numeric pain rating scale (NPRS). The NPRS is known to be a sensitive and reliable scale for clinical and experimental evaluation of pain intensity. The score ranges from 0, indicating no pain, to 10, expressing worst imaginable pain. The reliability of numeric pain rating scale (NPRS) is 0.92 (0.87, 0.95).
6 weeks
range of motion : universal goniometer
Universal Goniometer is the most commonly utilised clinical tool for measuring joint range of motion due to its ease of use, low cost, and demonstrated reasonable levels of reliability and validity in numerous studies. Validity and intertester reliability (r =.97-.98; ICC =.98-.99) are both high
6 weeks
shoulder pain and impairment : SPADI
The SPADI consists of 13 items that assess two domains: a 5-item subscale for pain and an 8-item subscale for disability. The SPADI has since been used in both primary care on mixed diagnosis and surgical patient populations including rotator cuff disease, osteoarthritis, and rheumatoid arthritis, adhesive capsulitis ,joint replacement surgery , and in a large population-based study of shoulder symptoms (37). Reliability- 0.89, Validity - 0.90
6 weeks
36-Item Short Form Health Survey questionnaire (SF-36)
The 36-Item Short Form Health Survey questionnaire (SF-36) is a very popular instrument for evaluating Health-Related Quality of Life. The ICC for SF-36 PF is (0.96, 95% CI 0.92-0.98) so it's a reliable test.
6 weeks
Assistente alla partecipazione
Criteri di eleggibilità

Età idonea
Adulto
Età minima
40 Years
Sessi idonei
Tutti
  • Age group 40-60 years
  • Male and female
  • Positive Capsular pattern (ER more limited than Abd which is more limited than IR)
  • Limitation in shoulder ROM ; Flexion <180 , Abduction <180 , External Rotation <50
  • Patients of stage 2 and 3 of adhesive capsulitis

  • History of surgery of the affected shoulder
  • Fractures in around the shoulder
  • Neurological disorders leading to altered muscle activity
  • Systemic arthritic conditions (RA, Osteoporosis)
  • Disorders of the cervical spine
Riphah International University logoUniversità internazionale Riphah416 studi clinici attivi da esplorare
Contatti principali dello studio
Contatto: Minal Mushtaq, MS-DPT, 03314662231, [email protected]
Contatto: Rabiya Noor, PHD, 03344355660, [email protected]
1 Centri dello studio in 1 paesi

Punjab Province

Johar Pain Relief Center, Lahore, Punjab Province, 54782, Pakistan
Rabiya Noor, Phd, Contatto, 03344355660, [email protected]
Minal Mushtaq, MS(OMPT), Investigatore principale
In arruolamento