- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT05115227
Long-term Multidisciplinary Team-based Management of Back Pain (TeamBack)
Long-term Multidisciplinary Team-based Management of Back Pain: Development and Feasibility (TeamBack Trial)
Long-term approaches are challenging to implement within the current care system, which rewards clinicians for attempting to quick-fix a long-term condition. This results in increased inappropriate imaging, opioid prescriptions, surgery, and visits/rehabilitation in secondary care, leading to higher societal costs and the continuing increase of LBP-related disability that is currently observed.
The investigators argue that LBP management can be optimized by providing patients with self-management strategies supported by a multidisciplinary team and providing simple, safe, and low-cost interventions that adhere to clinical guidelines. This has the potential to change patient behaviors and facilitate empowerment to self-manage LBP leading to lower societal costs of LBP.
Research objectives
The investigators will develop and test a long-term supportive multidisciplinary team-based management strategy with a specific focus on communicating a structured and unchanging message about individualized diagnosis, treatment, and prognosis, focusing on conducting a large randomized controlled trial as the next phase.
This feasibility trial will be completed in a secondary care settings, where relevant patients with poor management skills and insufficient effects of usual (primary) care management can be identified.
The specific objectives are:
(I) To develop a long-term supportive multidisciplinary team-based management strategy for secondary-care low back pain patients
(II) To test the feasibility by assessing:
- Changes in relevant outcomes
- Utilization of Primary care
- Patients and clinicians experience with the intervention
- Practical challenges of the setting
The management strategy development follows the principles provided by the Medical Research Council for developing complex interventions.
Development of the framework
Step 1: Framework setup
The investigators constructed a basic framework for the intervention by reviewing relevant systematic reviews and clinical guidelines. The research group determined the initial management intervention. Afterward, the investigators conducted a small survey on 191 participants (11% of the total sample of patients between February and May 2021), about their interest in participating. The majority would find such an approach of interest (147(77%)). In parallel, the investigators conducted short semi-structured interviews concerning the intervention with a convenient sample of 20 patients. Seventeen provided usable data.
Step 2 - Development
Using the participants' information, the investigators re-framed the management strategy. Subsequent semi-structured focus-group interviews with a clinical panel for further modifications before testing was conducted.
Step 3 - Feasibility
The multidisciplinary team for the feasibility trial consists of two coordinators (chiropractors), two therapists (physical therapists), one medical doctor, and one nurse.
The feasibility trial aims to identify and develop the appropriate framework by:
I) Investigating the patients' experiences of the current management strategy II) Ensuring satisfactory work-relations between clinicians III) Determining the primary outcome IV) Mapping the multiple interacting components of the management strategy V) Investigating how to measure parallel use of primary care and how this could be applied in the trial evaluation VI) Estimating the workload (number of hours) of the clinicians VII) Quantifying any out-of-protocol behaviors by clinicians and patients alike VIII) Quantifying the different aspects of the intervention using the clinical records
The feasibility trial will include 25 LBP patients from the Spine Centre willing to participate in a limited three-month follow-up.
The intervention procedure is:
1) A team meeting will be held each morning where the coordinator and the feasibility team will go through the patients. This will start the initial sparring process to ensure a structured and unchanging message for the patient.
The coordinator will first assess each patient face-to-face according to ICD-10 principles and enroll eligible patients in the trial. Afterward, the therapist will evaluate the patient's current functional status and management strategy. During the three months, patients will have multiple encounters with the coordinator, the therapist, and the nurse, if needed. The therapist will provide further interventions (e.g., exercise and cognitive/behavioral therapy) to encourage self-management.
The investigators will assess the following outcomes at three months: Disability (primary), pain, self-efficacy, quality of life, LBP trajectory, workability, and work retention.
Studienübersicht
Status
Bedingungen
Intervention / Behandlung
Studientyp
Einschreibung (Tatsächlich)
Phase
- Unzutreffend
Kontakte und Standorte
Studienorte
-
-
-
Middelfart, Dänemark, 5500
- Spine Centre of Southern Denmark
-
-
Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
Akzeptiert gesunde Freiwillige
Studienberechtigte Geschlechter
Beschreibung
Inclusion Criteria:
- Able to speak Danish
- Disability score > 40%
- Duration of current episode > 3 months
Exclusion Criteria:
- Surgical candidate due to acute radiculopathy
- Malignant or inflammatory back pain
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Behandlung
- Zuteilung: N / A
- Interventionsmodell: Einzelgruppenzuweisung
- Maskierung: Keine (Offenes Etikett)
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
|
Experimental: Multidisciplinary
A pragmatic team-based management approach is individualized for each patient.
|
The team will educate the patient about low back pain and how this can be self-managed.
Andere Namen:
The team will advice the patient to conduct relevant exercises and to stay physical active.
|
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Disability
Zeitfenster: Changes in mean values from baseline to 3 months
|
The Oswestry disability index
|
Changes in mean values from baseline to 3 months
|
Mitarbeiter und Ermittler
Sponsor
Ermittler
- Hauptermittler: Casper G Nim, PhD, Spine Center of Southern Denmark, University Hospital of Southern Denmark
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn (Tatsächlich)
Primärer Abschluss (Tatsächlich)
Studienabschluss (Tatsächlich)
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
- TeamBack
Plan für individuelle Teilnehmerdaten (IPD)
Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?
Beschreibung des IPD-Plans
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 Schmerzen im unteren Rücken
-
Brai²nRekrutierungNeurophysiologische Empfindlichkeit gegenüber Rückenmarksstimulation | Failed Back Surgery Syndrome (FBSS) | Persistent Spinal Pain Syndrome Typ 2 (PSPS-T) Untere WirbelsäuleBelgien
-
Brixton Biosciences, Inc.MCRANoch keine RekrutierungGreater Trochanteric Pain Syndrome | Seitliche Hüftschmerzen | Greater Trochanteric Pain Syndrome beider unteren Extremitäten
-
Kanuni Sultan Suleyman Training and Research HospitalRekrutierungGreater Trochanteric Pain SyndromeTürkei (türkiye)
-
Bozok UniversityAbgeschlossen
-
Foundation IRCCS San Matteo HospitalAktiv, nicht rekrutierendGreater Trochanteric Pain Syndrome beider unteren ExtremitätenItalien
-
Hager Montaser Sayed BedeerNoch keine RekrutierungRückenbrötchen Einschätzungen | Back Rolls Management
-
Health Services Academy, Islamabad, PakistanUnbekanntmGesundheit | Wiederaufnahme | Teach-Back-KommunikationPakistan
-
Future University in EgyptAbgeschlossen
-
Ankara Etlik City HospitalAbgeschlossenGluteale Tendinopathie | Greater Trochanteric Pain Syndrome | Tiefes Gluteal-SyndromTürkei (türkiye)
-
Camilo Jose Cela UniversityAbgeschlossenMyofascial Pain Syndrom (MPS)Spanien
Klinische Studien zur Education
-
Aydin Adnan Menderes UniversityRekrutierungSchwangerschaft | Ausbildung | Geburt | Geburtszufriedenheit | GeburtsgedächtnisTruthahn
-
Saglik Bilimleri UniversitesiAbgeschlossenPflegeausbildung | Frauengesundheit | Klimawandel | Nachhaltige EntwicklungTürkei (türkiye)
-
Istanbul Aydın UniversityAbgeschlossenStudenten der KrankenpflegeTürkei (türkiye)
-
Saglik Bilimleri UniversitesiAbgeschlossenHumanes Papillomavirus (HPV)Truthahn
-
National Yang Ming UniversityAbgeschlossenGesunde ErwachseneTaiwan
-
Riphah International UniversityAbgeschlossen
-
Saglik Bilimleri UniversitesiNoch keine Rekrutierung
-
National University of Ireland, Galway, IrelandUniversity College Hospital Galway; Brothers of Charity Services Galway IrelandNoch keine RekrutierungGeistige Behinderungen (F70-F79) | Krebsbewusstsein und Präventionserziehung | Bewusstsein für BrustkrebsIrland
-
Riphah International UniversityRekrutierungHemiplegie und HemiparesePakistan
-
University of FloridaAbgeschlossenDiabetes Typ 1 | Typ 2 DiabetesVereinigte Staaten