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Published on: July 27, 2018
Gaining information about home visits in primary care: methodological issues from a feasibility study
Karen Voigt1, Stephanie Taché, Andreas Klement
1Department of General Practice/Medical Clinic III, University Hospital Carl Gustav Carus of the Technische Universität Dresden, Fetscherstraße 74, 01307 Dresden, Germany. Karen.Voigt@uniklinikum-dresden.de.
A pilot study assessed the feasibility of documenting general practitioners' (GPs) home visits. Key challenges included GP time constraints and obtaining patient consent, particularly for those with cognitive impairments, highlighting areas for study design improvement.
Area of Science:
- Gerontology
- Primary Care Medicine
- Health Services Research
Background:
- Home visits are a crucial component of general practice in Germany.
- An aging population and a shortage of general practitioners (GPs) raise questions about care for immobile patients.
- A pilot study was conducted to assess the feasibility of a large-scale documentation study on GPs' home visits.
Purpose of the Study:
- To evaluate the feasibility of a documentation-intensive study on general practitioners' (GPs) home visits.
- To identify challenges and potential improvements for future research on primary care home visits.
- To assess the organizational aspects and content of GPs' home visits for immobile patients.
Main Methods:
- A mixed-methods design was employed with two study arms.
- The quantitative arm involved participating GPs and documentation of home visits.
- The qualitative arm explored reasons for non-participation among GPs.
Main Results:
- Common reasons for GP non-response included lack of time and interest; monetary incentives were not significant.
- Documentation rates varied, with discrepancies between documented and actual home visits.
- Obtaining patient consent was a major challenge, especially for patients with cognitive deficits.
Conclusions:
- The pilot study provides insights for refining study designs and instruments for future research on GP home visits.
- Improvements in instructions and questionnaires are planned to enhance data reliability.
- Addressing the inclusion of homebound patients unable to provide informed consent is critical for study representativeness.
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