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A Digital Support to Facilitate Sustainable Return to Work for Persons With Chronic Pain and Their Employers

An Evidence-based Digital Support for One Year to Facilitate a Sustainable Return to Work for Persons With Chronic Musculoskeletal Pain and Their Employers: Study Protocol for a Registry-based Multicentre Randomized Controlled Trial.

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05058547
Acronym
SWEPPE
Enrollment
360
Registered
2021-09-27
Start date
2022-03-01
Completion date
2024-12-31
Last updated
2022-03-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Pain

Keywords

collaboration support, eHealth, employer support, smartphone application, return to work, self-management

Brief summary

Chronic musculoskeletal pain (CMSP) severely affects the individual's quality of life, functioning and ability to work, and comes with significant societal costs for sick leave and loss of productivity. After completing an Interdisciplinary Pain Rehabilitation Program (IPRP), patients with CMSP experience a gap in the return to work (RTW) process when the responsibility for RTW is taken over by the employer. To fill this gap, we aim to evaluate the clinical effectiveness of a digital support (SWEPPE) for promoting a sustainable RTW for persons with CMSP and to facilitate the employers' supportive role and responsibilities in the process. Our hypothesis is that using SWEPPE will decrease the need for sick-leave. SWEPPE is a smartphone application where the individual can create an action plan, perform daily registrations of health aspects, self-monitoring of health aspects and goals, have access to a library with evidence-based facts and a coach, and the possibility to share information with the employer.The employer access SWEPPE via a web application. In this trial, we will recruit patients with CMSP aged 18-65 years who have completed IPRP, and who need support during RTW or continued support at the work placement for creating a sustainable work situation. The participants will be randomly assigned to either receive SWEPPE or to the control group. The intervention group will use SWEPPE during twelve months and the control group will not receive any active intervention for RTW which is standard clinical practice. Participants will be recruited from specialist and primary care level units connected to the Swedish National Quality Registry for Pain Rehabilitation (SQRP) and providing IPRP for patients with CMSP. All participants will fill in questionnaires when they have completed the rehabilitation program and before the intervention starts. Study ending assessment will be performed after twelve months. The clinical effectiveness of SWEPPE will be assessed by number of days with sickness cash benefit. Several dimensions of sick-leave will be assessed according to the Swedish Social Insurance Agency's (SSIA) proposal of outcome measures of RTW. Other outcomes and explanatory variables including important domains affected by CMSP such as health-related quality of life, functioning and work ability will be collected. A sample size calculation indicates the need for recruiting 360 participants (n=180 for each group).

Interventions

DEVICESWEPPE

In the smartphone application SWEPPE the individual can create an action plan, perform daily registrations of health aspects, self-monitoring of health aspects and goals, have access to a library with evidence-based facts and a coach, and possibility to share information with the employer.

Sponsors

Swedish Council for Working Life and Social Research
CollaboratorOTHER
Linkoeping University
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

Patients entering the trial must have completed IPRP. The principal inclusion criteria for IPRP in Sweden are: * persistent or intermittent pain lasting ≥3 months * pain affecting daily activities to a large extent, * completed systematic assessment and non-pharmacological optimization is completed, * screening for psychosocial risk factors and differential diagnosis completed In addition the following criteria will be applied: * Completed participation in an Interdisciplinary Pain Rehabilitation Program (IPRP) at any of the participating units. * Having an employment to return to after IPRP or having returned to work but need continued support for creating a sustainable work situation after IPRP.

Exclusion criteria

* Completed IPRP but are unemployed or unable to return to work.

Design outcomes

Primary

MeasureTime frameDescription
Sick leave12 months follow up after IPRPNumber of gross and net days with sickness cash benefit

Secondary

MeasureTime frameDescription
Sick-leave spells per months12 months follow up after IPRPNumber of sick-leave spells (per month)
Return to work group level12 months follow up after IPRPProportions of a group who returns to full- or part-time work (per month)
Working days before new sick leave12 months follow up after IPRPNumber of days in work before new sick leave during study period
Proportion back to work12 months follow up after IPRPProportion of a group back to work \>28 days (full- or part time) before a new sick-leave spell occurs
Total sick-leave spells12 months follow up after IPRPNumber of sick-leave spells during study period
Length of total sick leave12 months follow up after IPRPLength of total sick leave during study period
Pain intensity last 7 daysBaseline and 12 monthsNumeric rating scale
Consequences of pain on daily lifeBaseline and 12 monthsMultidimensional Pain Inventory Swedish version
Overall emotional distressBaseline and 12 monthsHospital Anxiety and Depression Scale Swedish version
Physical and mental healthBaseline and 12 monthsRAND-36 Swedish version
Goal fulfilment and satisfaction during the study periodBaseline and 12 monthsSelf-reported data
Self-reported physical work environmentBaseline and 12 monthsQuestionnaire based on the Swedish Work Environment Authority ergonomics checklist
Return to work12 months follow up after IPRPReturn to work (partially or full time) every month

Other

MeasureTime frameDescription
Self-reported level of sleep disturbanceBaseline and 12 monthsInsomnia Severity Index Swedish version
Self-reported fear of movementBaseline and 12 monthsTampa Scale for Kinesiophobia Swedish version
Self-reported physical activityBaseline and 12 monthsthe National Board of Health and Welfare's three questions on physical activity, exercise, and sedentary behavior.
Pain catastrophizingBaseline and 12 monthsPain Catastrophizing scale Swedish version
Perceived work abilityBaseline and 12 monthsWork Ability Index Swedish version
Self-reported demands, control, and support at the workplaceBaseline and 12 monthsDemand Control Support Questionnaire Swedish version
Perceived life SatisfactionBaseline and 12 monthsLife satisfaction Scale Swedish version
Self-reported work situation during the study periodBaseline and 12 monthsBarriers for return to work, strategies to handle barriers and need of support from the employer
Self-reported workload an average dayBaseline and 12 monthsNumber of hours per day for paid work and unpaid household work
Self-reported level of sleepinessBaseline and 12 monthsKarolinska Sleepiness Scale Swedish version
Self-reported fatigue the last 7 daysBaseline and 12 monthsNumeric rating scale

Countries

Sweden

Contacts

Primary ContactMathilda Björk, PhD
mathilda.bjork@liu.se+4611363531

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 12, 2026