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Impact of Digital Tools on Knowledge, Genetic Counseling, and Testing Uptake: A Systematic Review and Meta-analysis
Maide Nur Tümkaya1, Şeyma İnciser Paşalak2, Memnun Seven3
1Koc University Graduate School of Health Sciences, Nursing,Topkapı, İstanbul, Turkey.
Digital genetic tools effectively increase pretest counseling completion. While genetic testing uptake and knowledge outcomes are comparable to in-person care, these technologies expand access to genetic services.
Area of Science:
- Genetics
- Digital Health
- Healthcare Technology
Background:
- The integration of digital tools in healthcare is rapidly expanding.
- Genetic counseling traditionally involves in-person consultations.
- Assessing the efficacy of digital alternatives is crucial for improving access and patient outcomes.
Purpose of the Study:
- To systematically review and meta-analyze the impact of digital genetic tools on pretest counseling completion, genetic testing uptake, and patient knowledge.
- To compare the effectiveness of digital genetic services with traditional in-person care.
Main Methods:
- A systematic review and meta-analysis of 17 studies involving 6,714 participants.
- Searches conducted across major databases: PubMed, Web of Science, Ovid MEDLINE, CINAHL, and Scopus.
- Methodological quality assessed using Cochrane and Joanna Briggs Institute (JBI) critical appraisal checklists.
Main Results:
- Digital interventions significantly increased pretest counseling completion (Odds Ratio [OR] 2.07, 95% CI 1.22-3.51).
- Genetic testing uptake showed no significant difference between digital and in-person care (OR 1.30, 95% CI 0.80-2.10; P = .29).
- Knowledge outcomes were comparable for telehealth versus in-person, with some digital formats showing potential for greater gains, though not statistically significant.
Conclusions:
- Digital genetic tools are generally non-inferior to in-person care for knowledge and psychosocial outcomes.
- Digital genetic counseling is equivalent to in-person care for genetic test uptake.
- These tools enhance access to genetic services, with nurses playing a vital role in patient guidance and ensuring equitable access.
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