- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT03004989
Experiences of Participating in Return to Work Group Programmes (RTW-GP)
Experiences of Participating in Return to Work Group Programmes for People With Musculoskeletal Disorders: A Focus Group Study
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Description détaillée
For a representative sampling of experiences, participants who had participated in various groups over time in outpatient and inpatient groups in the RTW-GP were invited to enrol in the study. Other inclusion criteria were age between 25 and 65 years, different musculoskeletal diagnosis and that they should come from the rural district/city of residence.
The participants received requests by letter to participate in the focus group interview six months after the final group intervention, the same time as they were invited to a follow-up visit. Only a few men had participated in the RTW-GPs and none of them wanted to take part in the study.
All participants were given written and oral information about the study, the use of recording and transcribing devices, and their right to withdraw from the study at any time. The interviews were carried out after the participants gave written, informed consent.
Three focus group interviews were conducted: one with six participants, and two with five. One participant who could not participate in the focus group interview participated at an individual interview with the same questions as in the focus groups. The individual interview was conducted first and served as a test for the questions in the interview guide.
Interventions The participants of this study had participated in one of three different RTW-GPs. These programmes are designed to enable participants to proactively take action in their daily lives and in collaboration with employers achieve the best possible working conditions. All the group sessions are based on cognitive theory where attention, awareness and reflection on one's own work and life situation is important. Motivation is instilled by helping participants recognise opportunities for change. Participants set work-related goals and receive individual feedback from multidisciplinary personnel in addition to various group-based sessions with teaching, activities and exercises. The participants are referred to the programme by a rheumatologist or a member of the hospital's multidisciplinary team as soon as possible after starting sick-leave.
Type d'étude
Inscription (Réel)
Contacts et emplacements
Lieux d'étude
-
-
-
Lillehammer, Norvège, 2609
- Revmatismesykehuset
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-
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
Accepte les volontaires sains
Sexes éligibles pour l'étude
Méthode d'échantillonnage
Population étudiée
La description
Inclusion Criteria:
- Participating RTW-GP
- Musculoskeletal diagnoses
- From the rural district/city of residence
- Speaking Norwegian
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
Cohortes et interventions
Groupe / Cohorte |
Intervention / Traitement |
|---|---|
|
Programme 1
RTW group in day clinics
|
The participants of this study had participated in one of three different RTW-GPs.
These programmes are designed to enable participants to proactively take action in their daily lives and in collaboration with employers achieve the best possible working conditions.
All the group sessions are based on cognitive theory where attention, awareness and reflection on one's own work and life situation is important
Autres noms:
|
|
Programme 2
RTW group in day clinics for people with fibromyalgia
|
The participants of this study had participated in one of three different RTW-GPs.
These programmes are designed to enable participants to proactively take action in their daily lives and in collaboration with employers achieve the best possible working conditions.
All the group sessions are based on cognitive theory where attention, awareness and reflection on one's own work and life situation is important
Autres noms:
|
|
Programme 3
My work and I
|
The participants of this study had participated in one of three different RTW-GPs.
These programmes are designed to enable participants to proactively take action in their daily lives and in collaboration with employers achieve the best possible working conditions.
All the group sessions are based on cognitive theory where attention, awareness and reflection on one's own work and life situation is important
Autres noms:
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Patient experiences after participating at RTW-GP
Délai: May 2012 - November 2013
|
Focus group interviews
|
May 2012 - November 2013
|
|
Quality of life
Délai: May 2012 - November 2013
|
Focus group interviews
|
May 2012 - November 2013
|
|
Work ability
Délai: May 2012 - November 2013
|
Focus group interview
|
May 2012 - November 2013
|
Collaborateurs et enquêteurs
Parrainer
Collaborateurs
Les enquêteurs
- Chaise d'étude: Bente Hamnes, PhD, Revmatismesykehuset AS
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude
Achèvement primaire (Réel)
Achèvement de l'étude (Réel)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Estimation)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Estimation)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- 2012/7266 UiO
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .
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