- ICH GCP
- US Clinical Trials Registry
- Clinical Trial 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
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
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.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
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Lillehammer, Norway, 2609
- Revmatismesykehuset
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Participating RTW-GP
- Musculoskeletal diagnoses
- From the rural district/city of residence
- Speaking Norwegian
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
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
Other Names:
|
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
Other Names:
|
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
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Patient experiences after participating at RTW-GP
Time Frame: May 2012 - November 2013
|
Focus group interviews
|
May 2012 - November 2013
|
Quality of life
Time Frame: May 2012 - November 2013
|
Focus group interviews
|
May 2012 - November 2013
|
Work ability
Time Frame: May 2012 - November 2013
|
Focus group interview
|
May 2012 - November 2013
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Study Chair: Bente Hamnes, PhD, Revmatismesykehuset AS
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2012/7266 UiO
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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