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Does the Knowledge of a "Non-return to Work" Predictive Score Influence Vocational Rehabilitation? (WORRK)

C

Clinique Romande de Readaptation

Status

Completed

Conditions

Pain

Treatments

Other: Risk Score for non-return to work

Study type

Interventional

Funder types

Other
NETWORK

Identifiers

NCT02396173
CliniqueRR-03

Details and patient eligibility

About

Background: Orthopaedic trauma are a leading cause of long-lasting sick-leave and persistent disability. People suffering from persistent sick-leave often need vocational rehabilitation (VR). Vocational programs are planned to improve the likelihood of returning to work (RTW). Physical conditioning, professional evaluation and training, as well as psychological and social interventions are the core of the treatments. Efficiency of these programs is moderate and there is scope for improvements. For instance, rehabilitation programs tailored to the individual needs and potentials are called for. However, the allocation remains difficult. Decision-supportive tools may be convenient to achieve this goal. Recently, the WORRK model was proposed to assess early on the risk of non-returning to work for those patients. The main goal of this research is to measure if the WORRK model improves patients' allocation to different vocational programs according to their "non-return to work" risk.

Full description

Methods:

Vocational inpatients after orthopaedic trauma (n=280), aged between 18-60 years. Three different vocational pathways can be selected: Simple (for patients with low "non-return to work" risk, 5 weeks stay), Coaching (intermediate risk, 5 weeks), Evaluation (high risk, 3 weeks). Design: randomized-controlled trial. In the intervention group, the probability not to return to work estimated with the WORRK model will be offered to the clinician team before the allocation decisions. In the control group, the probability will also be estimated but not known by the clinician team. The primary outcome is the proportion of patients allocated to the Evaluation Pathway. Secondary outcomes: the patients' satisfaction is not worse in the intervention group; the decisions makers' satisfaction with the information available for the decision process is better in the intervention group; the proportion of patients changing the treatment pathway during the vocational stay is not higher in the intervention group; and the calibration of the WORRK model remains satisfactory; the non-return to work rate is not higher in the intervention group than in the control group (follow-up at 3, 12, and 24 months);

Relevance and impact:

The investigators expect that the WORRK model will improve the efficiency of vocational rehabilitation after orthopedic trauma. This will due to better allocation to the vocational pathways according to the patients' risk profile. If this is the case, an increase of the shorter vocational program is expected without jeopardizing the chance of returning to work and the patient satisfaction with quality of care. The ability of the WORRK model to detect patients with similar risk profiles could also strengthen the interest for this decision-supportive tool in clinical practice and trials.

Enrollment

280 patients

Sex

All

Ages

18 to 62 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients hospitalized for a vocational rehabilitation programme after an orthopaedic trauma

Exclusion criteria

  • Severe traumatic brain injury at time of accident (Glasgow coma Scale ≤8)
  • Spinal Cord Injury
  • Not capable of judgment
  • Under legal custody

Trial design

Primary purpose

Screening

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

280 participants in 2 patient groups

Risk Score for non-return to work
Experimental group
Description:
The WORRK model is a predictive tool (19 items) of the non-return to work risk useful for all kinds of orthopaedic trauma and for patients needing vocational rehabilitation. It is constructed with variables independent of the patient's education and language fluency. It is a short patient's bedside tool and takes less than 20 minutes.
Treatment:
Other: Risk Score for non-return to work
Control group
No Intervention group
Description:
In this group the medical staff will not be informed about the risk score (WORRK).

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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