- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico 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
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Descripción detallada
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.
Tipo de estudio
Inscripción (Actual)
Contactos y Ubicaciones
Ubicaciones de estudio
-
-
-
Lillehammer, Noruega, 2609
- Revmatismesykehuset
-
-
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Método de muestreo
Población de estudio
Descripción
Inclusion Criteria:
- Participating RTW-GP
- Musculoskeletal diagnoses
- From the rural district/city of residence
- Speaking Norwegian
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
Cohortes e Intervenciones
Grupo / Cohorte |
Intervención / Tratamiento |
---|---|
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
Otros nombres:
|
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
Otros nombres:
|
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
Otros nombres:
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
---|---|---|
Patient experiences after participating at RTW-GP
Periodo de tiempo: May 2012 - November 2013
|
Focus group interviews
|
May 2012 - November 2013
|
Quality of life
Periodo de tiempo: May 2012 - November 2013
|
Focus group interviews
|
May 2012 - November 2013
|
Work ability
Periodo de tiempo: May 2012 - November 2013
|
Focus group interview
|
May 2012 - November 2013
|
Colaboradores e Investigadores
Patrocinador
Colaboradores
Investigadores
- Silla de estudio: Bente Hamnes, PhD, Revmatismesykehuset AS
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio
Finalización primaria (Actual)
Finalización del estudio (Actual)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Estimar)
Actualizaciones de registros de estudio
Última actualización publicada (Estimar)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- 2012/7266 UiO
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .