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Short- and Medium-term Outcomes of the 3- Versus 4-week PV RehaJET® Rehabilitation Programme

Kurz- Und Mittelfristige Outcomes Des 3- Versus 4-wöchigen PV RehaJET® Erstheilverfahrens

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07700017
Enrollment
499
Registered
2026-07-13
Start date
2026-07-07
Completion date
2026-07-07
Last updated
2026-07-13

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

Conditions

Musculoskeletal Diseases or Conditions

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.

Detailed description

Secondary Data Analysis

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.

Sponsors

Pensionsversicherungsanstalt
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* 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

Exclusion criteria

* 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)

Design outcomes

Primary

MeasureTime frameDescription
IMBA - Profile comparison3 or 4 weeks of inpatient rehabilitationIMBA 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.
Employment history6 months after finishing rehabilitationThe 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.

Secondary

MeasureTime frameDescription
Work ability index (WAI)3 or 4 weeks of inpatient rehabilitationThe Work Ability Index (WAI) is an instrument for assessing work ability. (Min. = 7, Max = 49). Lower values indicate less subjective work ability.
Patient Health Questionnaire-4 (PHQ-4)3 or 4 weeks of inpatient rehabilitationThe Patient Health Questionnaire-4 (PHQ-4) operationalizes core criteria for anxiety and depression on a 4 point likert scale (Min. = 0, Max = 4). Lower values indicate less impairments.
European Quality of Life 5 Dimensions 5 Level (EQ-5D-5L)3 or 4 weeks of inpatient rehabilitationThe EQ-5D-5L is a general instrument for measuring patient-reported outcomes (PROs), which can be used to assess the quality of life of patients on different dimensions (mobility, self-care, usual activities, pain/discomfort) on a 5-level scale (Min. = 0, Max. = 5). Lower values indicate less impairments in the respective dimensions. Moreover, the EQ-5D-5L assesses the patient's self-rated health on a 100 point visual analog scale (Min. = 0, Max. = 100). Lower values indicate less positive ratings of health.

Countries

Austria

Contacts

STUDY_CHAIRDoreen Stöhr, Mag.

Pensionsversicherungsanstalt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 14, 2026