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Completed

NCT Number: NCT03004989

Experiences of Participating in Return to Work Group Programmes

To explore the experiences of individuals with musculoskeletal disorders (MSDs) who have participated in return-to-work group programmes (RTW-GPs) and see how the programmes could strengthen their work ability.

Completed

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Key information

Age range

28 year–57 year

Sex eligibility

Female

Study type

Observational

Primary location

Revmatismesykehuset

Lillehammer, 2609, Norway

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Participating RTW-GP
  • Musculoskeletal diagnoses
  • From the rural district/city of residence
  • Speaking Norwegian

Treatment and study plan

Programme

Behavioral

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 1, Programme 2, Programme 3

Primary outcomes

  1. Patient experiences after participating at RTW-GP

    Time frame: May 2012 - November 2013

    Focus group interviews

  2. Quality of life

    Time frame: May 2012 - November 2013

    Focus group interviews

  3. Work ability

    Time frame: May 2012 - November 2013

    Focus group interview

Sponsors and collaborators

Lead sponsor

Revmatismesykehuset AS

Other

Collaborators

  • South-Eastern Norway Regional Health Authority

Registry information

Official study title

Experiences of Participating in Return to Work Group Programmes for People With Musculoskeletal Disorders: A Focus Group Study

Acronym: RTW-GP

Important dates

Study start
2012
Primary completion
2013
Study completion
2016
First posted
Dec 29, 2016
Registry last updated
Jan 2, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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