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Experiences of Participating in Return to Work Group Programmes (RTW-GP)

30 december 2016 uppdaterad av: Revmatismesykehuset AS

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

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.

Studieöversikt

Status

Avslutad

Intervention / Behandling

Detaljerad beskrivning

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.

Studietyp

Observationell

Inskrivning (Faktisk)

17

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studieorter

      • Lillehammer, Norge, 2609
        • Revmatismesykehuset

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

28 år till 57 år (Vuxen)

Tar emot friska volontärer

Nej

Kön som är behöriga för studier

Kvinna

Testmetod

Icke-sannolikhetsprov

Studera befolkning

A total of 17 female informants participated in the study, age 28 - 57 years

Beskrivning

Inclusion Criteria:

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

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

Kohorter och interventioner

Grupp / Kohort
Intervention / Behandling
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
Andra namn:
  • Programme 1
  • Programme 2
  • Programme 3
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
Andra namn:
  • Programme 1
  • Programme 2
  • Programme 3
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
Andra namn:
  • Programme 1
  • Programme 2
  • Programme 3

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Patient experiences after participating at RTW-GP
Tidsram: May 2012 - November 2013
Focus group interviews
May 2012 - November 2013
Quality of life
Tidsram: May 2012 - November 2013
Focus group interviews
May 2012 - November 2013
Work ability
Tidsram: May 2012 - November 2013
Focus group interview
May 2012 - November 2013

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Utredare

  • Studiestol: Bente Hamnes, PhD, Revmatismesykehuset AS

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart

1 maj 2012

Primärt slutförande (Faktisk)

1 november 2013

Avslutad studie (Faktisk)

1 januari 2016

Studieregistreringsdatum

Först inskickad

20 december 2016

Först inskickad som uppfyllde QC-kriterierna

28 december 2016

Första postat (Uppskatta)

29 december 2016

Uppdateringar av studier

Senaste uppdatering publicerad (Uppskatta)

2 januari 2017

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

30 december 2016

Senast verifierad

1 december 2016

Mer information

Termer relaterade till denna studie

Ytterligare relevanta MeSH-villkor

Andra studie-ID-nummer

  • 2012/7266 UiO

Plan för individuella deltagardata (IPD)

Planerar du att dela individuella deltagardata (IPD)?

NEJ

Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .

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