- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05493306
Evaluation of Telerehabilitation Following Inpatient or Outpatient Rehabilitation Phase II
Evaluation Der Telerehabilitation im Anschluss an Eine stationäre Oder Ambulante Rehabilitation Phase II - Pilotprojekt [Evaluation of Telerehabilitation Following Inpatient or Outpatient Rehabilitation Phase II - Pilot Project]
Telerehabilitation is implemented in the Pensionsversicherungsanstalt (PVA) as an independent rehabilitation offer following a rehabilitation phase II. This offer primarily includes physiotherapeutic training units in group settings and in individual counselling, as well as health-related educational sessions and doctor's consultations via video conferencing, initially for rehabilitation patients with diseases of the musculoskeletal system or oncological diseases. The first stage of the implementation process was evaluated with a focus on acceptance, usability and feasibility from the perspective of patients and treatment team.
The evaluation was based on a convergent mixed methods design (Creswell & Plano Clark, 2017) to draw on the strengths of qualitative and quantitative research approaches (Creswell & Creswell, 2018). Qualitative and quantitative data were generated in parallel and treated equally. The perspective of the patients (N = 86) was collected through online questionnaires and in-depth telephone interviews (N = 22) and that of the treatment team through a questionnaire survey (N = 32) and focus group interviews (N = 24). The administrative team (N = 8) was asked for their assessment in a focus group interview. Technical difficulties in the implementation of telerehabilitation were documented by the treatment team. The consolidation of these multi-perspective results took place at the level of interpretation.
Study Overview
Status
Conditions
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
Styria
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Graz, Styria, Austria, 8020
- PVA - Zentrum für ambulante Rehabilitation Graz
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
Patients who have completed rehabilitation (phase II) with the indications:
- musculoskeletal diseases
- oncology.
Exclusion Criteria:
- Failure to obtain the declaration of consent
- Lack of the required technical aids (mobile phone, tablet or PC)
- Lack of the technical skills to operate the app and thus to participate in telerehabilitation.
Study Plan
How is the study designed?
Design Details
- Observational Models: Other
- Time Perspectives: Prospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Usability of the telerehabilitation
Time Frame: April 2021 - May 2022
|
The patients' perspective was collected with a self-developed online questionnaire (N = 86) and in-depth telephone interviews (N = 22). The questionnaires were analysed descriptively. The telephone interviews were protocolled and subsequently coded and categorised. The perspective of the treatment team was collected with a self-developed questionnaire (N = 32) and focus group interviews (N = 24). In addition, the administrative team (N = 8) was asked for their assessments in a focus group interview. The questionnaires were analysed descriptively. The focus group interview was recorded and subsequently coded and categorised. |
April 2021 - May 2022
|
Feasibility of the telerehabilitation
Time Frame: April 2021 - May 2022
|
Technical difficulties concerning the video calls were continuously documented by the treatment team.
The data were analysed descriptively.
|
April 2021 - May 2022
|
Acceptance of the telerehabilitation
Time Frame: April 2021 - May 2022
|
The patients' perspective was collected with a self-developed online questionnaire (N = 86) and in-depth telephone interviews (N = 22). The questionnaires were analysed descriptively. The telephone interviews were protocolled and subsequently coded and categorised. The perspective of the treatment team was collected with a self-developed questionnaire (N = 32) and focus group interviews (N = 24). The questionnaires were analysed descriptively. The focus group interviews were recorded and subsequently coded and categorised. |
April 2021 - May 2022
|
Collaborators and Investigators
Sponsor
Investigators
- Study Chair: David Felder, Mag., Pensionsversicherungsanstalt
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 0002 Evaluation Telereha
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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