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PAINTEAM

Interdisciplinary rehabilitation for chronic pain in primary healthcare
Source : Importé depuis le centre

Référence clinicaltrials.gov: NCT06084390
randomised controlled trial
primary care
Source : Importé depuis le centre
Recrutement fermé
Dernière modification : 2025/04/03
Type de recherche

Interventionnel


Population cible

Condition médicale (spécialité visée)

Donnée non disponible

Profil des participants

Sexe(s) des participants

ALL

Source : Importé depuis le centre

Critères de sélection

Critères d'inclusion

Inclusion Criteria:

* Persons participating in interdisciplinary team rehabilitation in primary healthcare in Region Västra Götaland, Sweden.

Exclusion Criteria:

* Severe psychiatric disease, language difficulties that makes it impossible to complete the questionnaires

Source : Importé depuis le centre

Thérapie ou Intervention proposée

Cohortes
Nom Condition médicale Traitement État du recrutement
Interdisciplinary rehabilitation + booster-session (intervention) Standard care by the interdisciplinary rehabilitation teams in primary healthcare + extended access to the team and a booster visit after 3 months. Donnée non disponible
  • Inconnu
  • Interdisciplinary rehabilitation (control) Standard care by the interdisciplinary rehabilitation teams in primary healthcare. Donnée non disponible
  • Inconnu
  • Interdisciplinary rehabilitation + booster-session (intervention)
    État du recrutement
    unknown
    Interdisciplinary rehabilitation (control)
    État du recrutement
    unknown
    Données à jour depuis : 3 avril 2025

    Description de l'étude

    Résumé de l'étude

    Purpose: The overall aim is to investigate the effect of interdisciplinary rehabilitation in primary health care (PHC) for patients with chronic pain. Specific questions: What is the effect of extended access to the interdisciplinary PHC pain team + a booster session after finishing the rehabilitation program? Does participation in PHC interdisciplinary rehabilitation contribute to health improvements and are there predictors of this? Method: A randomized controlled trial (RCT). 200 patients with chronic pain that participate in interdisciplinary rehabilitation in primary healthcare in Region Västra Götaland (VGR) in Sweden will be included in the RCT and randomized to Intervention; standard care by the interdisciplinary teams in PHC + extended access to the team and a booster session 3 months after the end of the rehabilitation, or Control; only standard care by the interdisciplinary teams. Outcomes are health related quality of life, pain intensity and other health aspects.

    Source : Importé depuis le centre

    The participants will be randomly allocated to intervention or active control. All participants in both arms receive the standard care for interdisciplinary rehabilitation at any of the six PHC pain teams in VGR. The teams consist of a physician, physiotherapist, occupational therapist and psychologist. All teams provide person-centred rehabilitation, aiming to increase physical activity and support behavioural changes, and to decrease symptoms and the impact of pain on the patients´ daily lives. The standard care interdisciplinary rehabilitation period contains both theoretical and practical components such as patient education, physical exercise and behavioural interventions. The sessions are mainly group-based. The duration of the rehabilitation period varies between 5 to 7 weeks + a follow-up visit after 3 months.

    The participants in the intervention arm also receive an extra booster-session 3 months after the standard follow-up. At the booster-session, the participant´s individual rehabilitation plan is followed-up and adjusted. This extra period also includes extended access to the team, meaning that the participants have the possibility to contact the team and, if needed, have digital or telephone contact.

    The participants complete a battery of questionaires included in the Swedish Quality Registry for Pain Rehabilitation an also extra questionnaires provided to the participants through an electronic research form.

    Data collection is made at baseline before starting the rehabilitation, directly after the 5 to 7 weeks rehabilitation period and 6, 12 and 24 months after baseline.

    Source : Importé depuis le centre

    Sites

    Centres participants

      1 centres
    • RESEARCH AND DEVELOPMENT PRIMARY HEALTH CARE FYRBODAL

      Vänersborg

      REGION VÄSTRA GÖTALAND, SWEDEN

      Recrutement local
      État du recrutement: FERMÉ

    Dernière modification : 3 avril 2025
    Données à jour depuis : 7 avr.
    Origine des données : clinicaltrials.gov
    Référence clinicaltrials.gov: NCT06084390