2023
DOI: 10.1016/j.jclinepi.2022.12.006
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A systematic scoping review of just-in-time, adaptive interventions finds limited automation and incomplete reporting

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Cited by 4 publications
(8 citation statements)
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“…Compared with reports of randomized clinical trials that assessed JITIs, the FDA databases contained less information on aspects associated with the decision and delivery components. We also found little overlap in the JITIs assessed in RCTs and JITIs approved by the FDA within the last 3 years, but this might only reflect a time-lag between study publication and market approval …”
Section: Discussionmentioning
confidence: 99%
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“…Compared with reports of randomized clinical trials that assessed JITIs, the FDA databases contained less information on aspects associated with the decision and delivery components. We also found little overlap in the JITIs assessed in RCTs and JITIs approved by the FDA within the last 3 years, but this might only reflect a time-lag between study publication and market approval …”
Section: Discussionmentioning
confidence: 99%
“…We developed a standardized extraction form (eMethods 3 in the Supplement). 1,15,[30][31][32] Two reviewers (N.T.T.P and T.O.) independently extracted a random sample of 53% of the product summaries.…”
Section: Data Extractionmentioning
confidence: 99%
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“…It is into this new era that just-in-time interventions (JITIs) were launched, integrating software in the form of DHTs with existing medical devices, including medication delivery devices and real-time contextual information to prompt users to take certain actions, or in some cases, to perform those actions directly. 3 By becoming patient context-specific, JITIs increased their theoretical power. 4 For example, JITIs may remind patients to take medications at the proper time, administer insulin from an implanted pump when the monitor indicates glucose levels are high, and discourage users from going into a corner store where they typically buy high-sugar food products.…”
mentioning
confidence: 99%