Development of a Research Agenda for Rehabilitation Research

March 6, 2025 updated by: Pensionsversicherungsanstalt

Entwicklung Einer Forschungsagenda Für Die Reha-Forschung in Der Österreichischen Pensionsversicherungsanstalt (PVA) [Development of a Research Agenda for Rehabilitation Research in the Austrian Pension Insurance Institution (PVA)]

An internal research department was established in the course of an organisational reform of the Pension Insurance Institution in 2020 for the evidence-based development of its own services in Austria. The focus is on the transfer of findings into practice and the scientific community. As part of an initial assessment of the current situation, an organisation-specific research agenda is being systematically developed.

The project design is based on a multi-perspective and multi-method approach. After obtaining experts' opinions (interview) from different settings and areas, a consensus on necessary fields of action will be worked out after synthesising the results via a Delphi survey.

Study Overview

Study Type

Observational

Enrollment (Actual)

163

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Vienna, Austria, 1021
        • Pensionsversicherungsanstalt

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

No older than 99 years (Child, Adult, Older Adult)

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

International and Austrian experts from science and research related to rehabilitation, cooperation partners, representatives of the rehabilitation facilities of the PVA, as well as decision-makers of the PVA were included.

Description

Inclusion Criteria:

  • Researchers who conduct scientific research in the field of rehabilitation in Austria, Germany and Switzerland
  • People working in rehabilitation facilities (in therapy or administration) in Austria, Germany and Switzerland

Exclusion Criteria:

  • Failure to obtain the declaration of consent

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: Other
  • Time Perspectives: Other

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Identification of priorities in applied rehabilitation research
Time Frame: April 2021 - November 2021

Semi-structured, guideline-based expert interviews with representatives of different stakeholder groups from Austria, Germany and Switzerland are conducted.

The transcribed interviews are extracted and evaluated within the framework of a qualitative content analysis according to Gläser & Laudel (2010).

Additionally, based on a scoping review on international research priorities and research agendas in the context of rehabilitation, potentially not considered content will be identified and supplemented.

April 2021 - November 2021
Weighting of the identified priorities in research
Time Frame: May 2023 - August 2023
A Delphi survey is conducted with (1) the interview partners and rehabilitation researchers and (2) other representatives of different stakeholder groups from Austria, Germany and Switzerland to evaluate the priorities of the developed research field. The experts are consulted repeatedly until a consensus can be obtained.
May 2023 - August 2023

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Doreen Stöhr, Mag., Pensionsversicherungsanstalt

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

April 1, 2021

Primary Completion (Actual)

August 1, 2023

Study Completion (Actual)

December 22, 2023

Study Registration Dates

First Submitted

August 4, 2022

First Submitted That Met QC Criteria

August 8, 2022

First Posted (Actual)

August 10, 2022

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

March 6, 2025

Last Verified

January 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • 0004 Masterplan Reha-Forschung

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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