- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT07786402
Clinical Outcomes of Prone and Supine Lumbar Traction Matched to Mechanical Bias in Flexion and Extension Subgroups With Lumbosacral Radiculopathy
Clinical Outcomes of Prone and Supine Lumbar Traction Matched to Mechanical Bias in Flexion and Extension Subgroups With Lumbosacral Radiculopathy.
Studienübersicht
Status
Bedingungen
Intervention / Behandlung
Studientyp
Einschreibung (Geschätzt)
Phase
- Unzutreffend
Kontakte und Standorte
Studienkontakt
- Name: Atef abdulalim nadier, Assistant professor
- Telefonnummer: +201003867064
- E-Mail: a.nadier@ammanu.edu.jo
Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
- Erwachsene
Akzeptiert gesunde Freiwillige
Beschreibung
Inclusion Criteria:
- Acute and subacute lumbosacral disc herniation with radiculopathy.
- Positive Straight leg raising test or Slump test.
Exclusion Criteria:
- Spondylolisthesis, prior spinal surgery, "Red Flags" (Cauda Equina, malignancy), or a non-mechanical response to repeated movements and patients with LBP without radiculopathy.
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Behandlung
- Zuteilung: Zufällig
- Interventionsmodell: Parallele Zuordnung
- Maskierung: Single
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
|
Experimental: A) Extension bias, prone traction
Mechanical intermittent traction will done for 15 minutes with patient in prone position, after release the patient let wrest for 2 minutes then asked to walking for 1 minutes without immediate sitting post traction period. Prone on elbow press up exercise . Infrared radiation on back before traction |
Press up on elbow exercise traction from prone.
|
|
Experimental: B) Extension bias, supine traction
Mechanical intermittent traction will done for 15 minutes with patient in supine position, after release the patient let wrest for 2 minutes then asked to walking for 1 minutes without immediate sitting post traction period. Infrared on back before the traction. Press up on elbow exercise . |
Press up on elbow exercise.
traction from supine
|
|
Experimental: C) Flexion bias, supine traction
Mechanical intermittent traction will done for 15 minutes with patient in supine position(matches flexion bias), after release the patient let wrest for 2 minutes then asked to walking for 1 minutes without immediate sitting post traction period. Infrared on the back before the traction for 10 minutes. Knee to chest exercise for 2 minutes before the session . |
Traction from supine with flexion bias exercise knee to chest exercise for 2 minutes
|
|
Experimental: D) Flexion bias, prone traction
Mechanical intermittent traction will done for 15 minutes with patient in prone position(mismatches flexion bias), after release the patient let wrest for 2 minutes then asked to walking for 1 minutes without immediate sitting post traction period. Infrared on the back before the traction for 10 minutes. Knee to chest exercise for 2 minutes before the session . |
Traction from prone with flexion bias exercise knee to chest exercise for 2 minutes
|
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Numerical pain scale (NPRS)
Zeitfenster: Pain intensity was assessed at baseline (during the initial assessment) and again after completion of the 12th treatment session (one-month follow-up)
|
Pain (lower limb radiating pain)
|
Pain intensity was assessed at baseline (during the initial assessment) and again after completion of the 12th treatment session (one-month follow-up)
|
|
Oswestry back scale (ODI)
Zeitfenster: Patients completed the ODI questionnaire at baseline during their initial clinical evaluation. A subsequent assessment was conducted upon completion of the 12-session intervention protocol (representing the one-month follow-up)
|
Functional questionnaire for back disability
|
Patients completed the ODI questionnaire at baseline during their initial clinical evaluation. A subsequent assessment was conducted upon completion of the 12-session intervention protocol (representing the one-month follow-up)
|
|
Hip flexion Angle
Zeitfenster: Hip flexion Angle was assessed at baseline (during the initial assessment) and again after completion of the 12th treatment session (one-month follow-up)
|
Hip flexion Angle during SLR test is also used to measure neural tension improvements for extension bias groups (by digital inclinometer)
|
Hip flexion Angle was assessed at baseline (during the initial assessment) and again after completion of the 12th treatment session (one-month follow-up)
|
|
Knee extension angle
Zeitfenster: Knee extension angle was assessed at baseline (during the initial assessment) and again after completion of the 12th treatment session (one-month follow-up)
|
Knee extension angle with active knee extension during slump test was used for flexion bias groups (to measure how many degrees the knee is away from full extension when the leg pain starts).
|
Knee extension angle was assessed at baseline (during the initial assessment) and again after completion of the 12th treatment session (one-month follow-up)
|
Mitarbeiter und Ermittler
Sponsor
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn (Geschätzt)
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
Andere Studien-ID-Nummern
- 1985
Plan für individuelle Teilnehmerdaten (IPD)
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Arzneimittel- und Geräteinformationen, Studienunterlagen
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