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Effects of Motivational Interviewing for Long-term Sick Absence

Not Applicable
Completed
Conditions
Sick Leave
Interventions
Behavioral: Structured talks (TAU-2)
Behavioral: motivational interviewing (MI)
Behavioral: Treatment as usual (TAU-0)
Registration Number
NCT03212118
Lead Sponsor
Norwegian University of Science and Technology
Brief Summary

Long-term sickness absence has considerable impact on social functioning, families involved, the employer, and society as a whole. Preventing long-term sickness absence and increase the likelihood of return to work (RTW) are critical concerns for industrialized countries across the world. Motivational factors contributing to RTW and maintenance of work participation are therefore of importance to explore in order to get the person back to work after long-term sick leave. Motivational interviewing (MI) is an empirically validated psychological approach that may be particularly useful in a RTW context. Even though MI has been widely studied and is considered a flexible intervention strategy in different domains, its effectiveness in improving RTW has not yet been studied.

The aim of this study is to evaluate whether MI provided by trained caseworkers at The Norwegian Labour and Welfare Administration (NAV) to sick-listed users with unselected diagnoses facilitates RTW compared with follow-up as usual.

Detailed Description

The main study will be preceded by a pilot study (anticipated start medio august 2017). The aim of the pilot is to test the practical aspects of the study. If no changes are made to the study protocol, the intervention or one of the other arms, participants from the pilot will be included in the main study, In case of modifications to the study protocol after the pilot, participants from the pilot study will not be included in the main study. Data for primary and secondary outcomes will not be assessed before the end of the main study.

In addition to the intention to treat and per protocol analyses, subgroup analyses will be performed if sufficient power for age, gender, diagnoses for sick leave, occupational category and length of previous sick leave.

In addition to the effect evaluation, qualitative studies, a feasibility/process evaluation study and a health economic evaluation (cost-effectiveness, cost-utility and cost-benefit) will be performed. The qualitative studies will be based on data from focus group discussions. The main areas for investigation will be:

* The participants' expectations to return to work before and after motivational interviewing.

* Perceived facilitators and obstacles for return to work among participants

* The perceived benefits and challenges in using motivational interview to facilitate a return to work process

Changes made Sept.29 2017: Due to slow recruitment, it was decided to leave out one of the arms from the study (TAU-1: extra phone call to employer). The extra phone call element was also taken out from the other arms where it was included. Another reason for this change was that the TAU-1 intervention arm was not ideally designed to evaluate the extra phone call. It was decided this intervention arm is better evaluated in a separate trial. Currently 12 persons are included and randomized in the trial. Those who are randomized to TAU-1 and have not received an intervention, will be randomized again. The ones randomized to TAU-1 who already have got an intervention will stop participating in the study.

Changes made Aug. 26 2019: Due to problems with implementation of the intervervention the first couple of months, it was decided to start inclusion from Jan 1st 2018 (instead of Aug 2017). The planned number of participants has not changed.

Clarification added April 25 2021. Regarding exclusion criterion unemployment: only sick listed individuals listed with an employer were identified in the sick leave registries and invited to take part in the study. That means individuals who were unemployed, self-employed or for other reasons without an employer were not included.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
774
Inclusion Criteria
  • Living in the county Sør-Trøndelag
  • On sick leave for 8 weeks
  • Current sick leave status of 50-100%
Exclusion Criteria
  • no employment
  • pregnancy

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Two talksStructured talks (TAU-2)Two standard talks (not including elements from motivational interviewing)
Motivational interviewingmotivational interviewing (MI)Two standard talks with a motivational interviewing content.
Treatment as usualTreatment as usual (TAU-0)Treatment as usual "untouched". This is the standard The Norwegian Labour and Welfare Administration (NAV) procedure.
Primary Outcome Measures
NameTimeMethod
Total number of sickness absence days during the year after enrollment in the study (i.e. after randomization)12 months

Register data from the national health and welfare services

Secondary Outcome Measures
NameTimeMethod
Return to work expectations12 months

Expectations about length of sick leave and return to work (3 items)

Probability of working (i.e. not receiving medical benefits) each month during follow-up, measured as repeated events12 months

Register data from the national health and welfare services

Resilience12 months

Resilience Scale for Adults (Friborg et al, 2003)

Workability12 months

Single question. How will you rate your work ability (scale from 0 (no ability) to 10 (my best ability)) (1 item)

The time until full sustainable return to work (RTW), i.e. for at least 4 weeks without relapse12 months

Register data from the national health and welfare services

Return to Work Self-Efficacy12 months

Return to Work Self-Efficacy Scale (Lagerveld et al, 2010)

Health-related quality of life12 months

EQ- 5D- 5L Questionnaire, Herdman et al, 2011

Trial Locations

Locations (1)

Dept

🇳🇴

Trondheim, Norway

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