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Comparison of Smart Display Versus Laptop Platforms for an eHealth Intervention to Improve Functional Health for Older Adults With Multiple Chronic Conditions: Protocol for a Randomized Clinical Trial

Comparison of Smart Display Versus Laptop Platforms for an eHealth Intervention to Improve Functional Health for Older Adults With Multiple Chronic Conditions: Protocol for a Randomized Clinical Trial

The PROMIS website also gives the mean and SD of the T-score metric (mean 50, SD 10). Power calculations for this primary hypothesis were performed using the SAS procedure PROC GLMPOWER (SAS Version 9.4) [62]. Results indicated that 282 participants after attrition would be needed for 80% power (P With regard to power for moderation analyses, we ran a sensitivity analysis to compute the smallest effect size our study would be powered to find using 280 given 4 groups (eg, 2 study arms × 2 genders).

David H Gustafson Sr, Marie-Louise Mares, Darcie C Johnston, John J Curtin, Klaren Pe-Romashko, Gina Landucci

JMIR Res Protoc 2025;14:e64449

Improving Early Dementia Detection Among Diverse Older Adults With Cognitive Concerns With the 5-Cog Paradigm: Protocol for a Hybrid Effectiveness-Implementation Clinical Trial

Improving Early Dementia Detection Among Diverse Older Adults With Cognitive Concerns With the 5-Cog Paradigm: Protocol for a Hybrid Effectiveness-Implementation Clinical Trial

The PMIS (Pearson r=−0.76; P As we examined the sensitivity and specificity data to choose cut scores, we chose to favor sensitivity to minimize missing individuals with true disease in this sample of patients considered high risk because of their cognitive concerns. The cut scores for a positive result on the 5-Cog components were as follows: PMIS ≤6 (range 0-8), Symbol Match ≤25 (range 0-65), and s MCR >5 (range 0-7).

Rachel Beth Rosansky Chalmer, Emmeline Ayers, Erica F Weiss, Nicole R Fowler, Andrew Telzak, Diana Summanwar, Jessica Zwerling, Cuiling Wang, Huiping Xu, Richard J Holden, Kevin Fiori, Dustin D French, Celeste Nsubayi, Asif Ansari, Paul Dexter, Anna Higbie, Pratibha Yadav, James M Walker, Harrshavasan Congivaram, Dristi Adhikari, Mairim Melecio-Vazquez, Malaz Boustani, Joe Verghese

JMIR Res Protoc 2025;14:e60471

Correction: Effect of Harm Anchors in Visual Displays of Test Results on Patient Perceptions of Urgency About Near-Normal Values: Experimental Study

Correction: Effect of Harm Anchors in Visual Displays of Test Results on Patient Perceptions of Urgency About Near-Normal Values: Experimental Study

In “Effect of Harm Anchors in Visual Displays of Test Results on Patient Perceptions of Urgency About Near-Normal Values: Experimental Study” (J Med Internet Res 2018;20(3):e98) the authors noted one error. In Table 2, the row labels for the 3 rows under “Extreme results” have been revised.

Brian J Zikmund-Fisher, Aaron M Scherer, Holly O Witteman, Jacob B Solomon, Nicole L Exe, Angela Fagerlin

J Med Internet Res 2025;27:e74908

Exploring Technical Features to Enhance Control in Videoconferencing Psychotherapy: Quantitative Study on Clinicians’ Perspectives

Exploring Technical Features to Enhance Control in Videoconferencing Psychotherapy: Quantitative Study on Clinicians’ Perspectives

No direct relationship was observed between “challenges in providing VCP” and “enhancing control” (r=0.16; P=.15). However, the factor “features to enhance TR” was moderately correlated with “enhancing control” (r=0.46; P Eigenvalue of the 3 factors. a Not available. Scree plot of the 4 factors loaded. The 3 factors loaded. a VCP: videoconference psychotherapy. b TR: therapeutic relationship. c Not applicable.

Francesco Cataldo, Shanton Chang, Antonette Mendoza, George Buchanan, Nicholas Van Dam

J Med Internet Res 2025;27:e66904

Cooperative Virtual Reality Gaming for Anxiety and Pain Reduction in Pediatric Patients and Their Caregivers During Painful Medical Procedures: Protocol for a Randomized Controlled Trial

Cooperative Virtual Reality Gaming for Anxiety and Pain Reduction in Pediatric Patients and Their Caregivers During Painful Medical Procedures: Protocol for a Randomized Controlled Trial

On the basis of a power analysis with the G*Power software [22] and starting from a 2-sided t test with a significance level of α=.05 and a test power of 80%, we determined that a medium-size effect of approximately Cohen d=0.64 can be achieved with a corresponding sample size of 39 participants per group.

Stefan Liszio, Franziska Bäuerlein, Jens Hildebrand, Carolin van Nahl, Maic Masuch, Oliver Basu

JMIR Res Protoc 2025;14:e63098