NCT07700017

Brief Summary

The objective of this observational study is to evaluate and compare the outcomes of two different durations of a recently established work-specific rehabilitation programme in Austria. The programme focuses on exercises tailored to patients' individual vocational needs. Two patient groups are observed: one group completes a three-week work-specific rehabilitation programme, while the other group completes a four-week work-specific rehabilitation programme, allowing a direct comparison of their outcomes.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
499

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jul 2026

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

July 7, 2026

Completed
Same day until next milestone

Study Start

First participant enrolled

July 7, 2026

Completed
Same day until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 7, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 7, 2026

Completed
6 days until next milestone

First Posted

Study publicly available on registry

July 13, 2026

Completed
Last Updated

July 13, 2026

Status Verified

July 1, 2026

Enrollment Period

Same day

First QC Date

July 7, 2026

Last Update Submit

July 7, 2026

Conditions

Outcome Measures

Primary Outcomes (2)

  • IMBA - Profile comparison

    IMBA is a profile comparison method for prevention and rehabilitation. Job requirements and human capabilities are described by standardised, defined characteristics and compared directly with each other. The respective profile sheets consist, among other things, of 70 function-, activity- and context-related main characteristics in which the extent of excessive demands for each characteristic is documented on a scale of 0 - 6 (Min. = 0, Max = 420). Lower values indicate less excessive demands.

    3 or 4 weeks of inpatient rehabilitation

  • Employment history

    The existence of gainful employment subject to social insurance contributions in a specific period allows conclusions to be drawn about the employment history of the rehabilitants.

    6 months after finishing rehabilitation

Secondary Outcomes (3)

  • Work ability index (WAI)

    3 or 4 weeks of inpatient rehabilitation

  • Patient Health Questionnaire-4 (PHQ-4)

    3 or 4 weeks of inpatient rehabilitation

  • European Quality of Life 5 Dimensions 5 Level (EQ-5D-5L)

    3 or 4 weeks of inpatient rehabilitation

Study Arms (2)

3-week work-specific rehabilitation

Patients participate in a 3-week work-specific rehabilitation programme with exercises tailored to their individual vocational and work-related needs.

Behavioral: Multimodal rehabilitation with additional work specific training

4-week work-specific rehabilitation

Patients participate in a 4-week work-specific rehabilitation programme with exercises tailored to their individual vocational and work-related needs.

Behavioral: Multimodal rehabilitation with additional work specific training

Interventions

The rehabilitation is based on the biopsychosocial ICF model of the WHO. Taking into account the physical and psychological condition of the patients, an individual therapy plan is created that is tailored to the needs of the patients.

Also known as: RehaJET
3-week work-specific rehabilitation4-week work-specific rehabilitation

Eligibility Criteria

Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patients with specific work-related rehabilitation needs

You may qualify if:

  • The study participants are patients undergoing the REHAJET programme
  • Presence of a disease in the area of the musculoskeletal system
  • Sufficient motivation to maintain professional participation

You may not qualify if:

  • No completion of all work-specific rehabilitation modules
  • Acute or decompensated disease states with severe functional limitations (i.e. not able to continue with the rehabilitation programme)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Pensionsversicherungsanstalt

Vienna, 1021, Austria

Location

MeSH Terms

Conditions

Musculoskeletal Diseases

Study Officials

  • Doreen Stöhr, Mag.

    Pensionsversicherungsanstalt

    STUDY CHAIR

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

July 7, 2026

First Posted

July 13, 2026

Study Start

July 7, 2026

Primary Completion

July 7, 2026

Study Completion

July 7, 2026

Last Updated

July 13, 2026

Record last verified: 2026-07

Locations