Early Identification of Risk for and Prevention of Sickness Absence Due to Musculoskeletal Pain - an RCT

NCT03913325 | Unknown

• 1 other identifier: FORTE 2018-01250
• Study Type: interventional
• Target: 254
• Locations: 1 country
• Sites: 1

Brief Summary

Background: Musculoskeletal pain is a leading cause of disability in the world. Although the majority of musculoskeletal-related pain conditions, such as low back pain, often resolves spontaneously, pain may recur or persist over a long time, potentially leading to disability and subsequent reduced work capacity and long-term sickness absence. There is a need for early identification of individuals in which this may occur, to prevent or reduce the risk of long-term musculoskeletal pain and long-term sickness absence. The aim of the trial described in this protocol is to evaluate a primary care rehabilitation model, PREVSAM, including early identification of patients at risk for long-term musculoskeletal pain and related sickness absence and a coordinated interdisciplinary rehabilitation programme based on individual and organizational resources. Methods: Eligible individuals will be recruited from primary care rehabilitation centres, health care centres, and include those who seek care for musculoskeletal pain and who are at risk of developing persistent pain, disability and sickness absence. Participants will be randomized to either treatment according to the PREVSAM model (intervention group) or treatment as usual (TAU) within primary care (control group). The PREVSAM model will comprise a person-centred rehabilitation plan, including coordinated measures within primary health care as well as in collaboration with participants' employers, and when relevant the Swedish Public Employment Agency. The primary outcome sickness absence will be measured at 3 and12 months from the Swedish Social Insurance Agency regarding: the number and proportion of individuals who remain in full- or part-time work, the number of gross and net days of sickness during the follow-up period, and time to first sickness absence spell. Secondary outcomes are patient-reported work ability, pain, health-related quality of life, risk for sickness absence, anxiety/depression, general and pain self-efficacy and disability at 3 months after inclusion (short-term follow-up), and at 6 and 12 months (long-term follow-up). Follow-up of drug consumption and cost-effectiveness analyes will be performed at 12 months. Discussion: This study is expected to provide new knowledge on how to best identify individuals at risk for long-term disability and sick leave due to musculoskeletal pain, and whether rehabilitation according to the PREVSAM model is effective. The study findings may contribute to more effective primary care rehabilitation processes of this large patient population, and potentially reduce sick leave and costs for healthcare and society.

Conditions

Musculoskeletal Disorder

Outcome Measures

Primary Outcomes (1)

• Registered sickness absence

  Registered sickness absence at Swedish Social Insurance Agency

  During 12 months from baseline

Secondary Outcomes (13)

• Short time sickness absence

  Weekly for 12 months following baseline

• Patient reported work ability

  At 1, 3, 6 and 12 months following baseline

• Risk of sickness absence assessed by Örebro Musculoskeletal Pain Screening Questionnaire Short Form (ÖMPSQ-SF)

  At 1, 3, 6 and 12 months following baseline

• Patient reported pain duration

  At 1, 3, 6 and 12 months following baseline

• Patient reported pain intensity

  At 1, 3, 6 and 12 months following baseline

Study Arms (2)

PREVSAM model

EXPERIMENTAL

Other: PREVSAM model

Treatment as usual

ACTIVE COMPARATOR

Other: Treatment as usual (standard treatment)

Interventions

PREVSAM model OTHER

A person-centred rehabilitation plan, including coordinated measures within primary health care as well as in collaboration with participants' employers, and when relevant the Swedish Public Employment Agency

PREVSAM model

Treatment as usual (standard treatment) OTHER

Treatment as usual (ordinary/standard) treatment. Can include unimodal or multimodal treatment of physiotherapy solely and/or occupational therapy

Treatment as usual

Eligibility Criteria

• Age: 18 Years - 100 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Aged over 18
• Musculoskeletal pain, preferably less than 3 months
• Risk for development of persistent musculoskeletal pain and disability ≥ 40 p on ÖMPSQ-SF
• Independently mobile (with or without aids), to be capable of participating in intervention

You may not qualify if:

• Pain not primarily generated from the musculoskeletal system
• Sickness cash benefit more than 30 days during the last 12 months due to pain from the musculoskeletal system
• Full disability pension
• Pregnancy
• Red flag disorders such as malignancy/cancer, acute traumas such as fracture (less than 6 months ago) or infection, spinal cord compression/cauda equina
• Severe mental illness

Sponsors & Collaborators

• Vastra Gotaland Region: lead
• Swedish Council for Working Life and Social Research: collaborator

Study Sites (1)

Research and Development primary care Region Västra Götaland

Gothenburg, Västra Götalandregionen, Sweden

Location

Related Publications (1)

• Larsson M, Nordeman L, Holmgren K, Grimby-Ekman A, Hensing G, Bjorkelund C, Bergman S, Ekhammar A, Dottori M, Bernhardsson S. Prevention of sickness absence through early identification and rehabilitation of at-risk patients with musculoskeletal pain (PREVSAM): a randomised controlled trial protocol. BMC Musculoskelet Disord. 2020 Nov 28;21(1):790. doi: 10.1186/s12891-020-03790-5.

  PMID: 33248457 DERIVED

MeSH Terms

Conditions

Musculoskeletal Diseases

Interventions

Therapeutics

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: DOUBLE
• Who Masked: INVESTIGATOR, OUTCOMES ASSESSOR
• Purpose: PREVENTION
• Intervention Model: PARALLEL
• Sponsor Type: OTHER GOV
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Associate Professor

Study Record Dates

• First Submitted: April 9, 2019
• First Posted: April 12, 2019
• Study Start: May 14, 2019
• Primary Completion: November 30, 2023
• Study Completion: December 30, 2024
• Last Updated: July 5, 2023

Record last verified: 2023-07

Locations

SE (1)