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Smartphone Ecological Momentary Assessment and Wearable Activity Tracking in Pediatric Depression: Cohort Study

Smartphone Ecological Momentary Assessment and Wearable Activity Tracking in Pediatric Depression: Cohort Study

Exclusion criteria for individuals with MDD included a severe neurodevelopmental disorder or other impairment that impacts the participant’s ability to provide the required information for the study (eg, symptom reports), a substance or medication-induced affective disorder, an affective disorder secondary to a medical condition, and a current Axis I psychotic or bipolar disorder.

Jimena Unzueta Saavedra, Emma A Deaso, Margot Austin, Laura Cadavid, Rachel Kraff, Emma E M Knowles

JMIR Form Res 2025;9:e66187

Screening and Risk Analysis of Atrial Fibrillation After Radiotherapy for Breast Cancer: Protocol for the Cross-Sectional Cohort Study “Watch Your Heart (WATCH)”

Screening and Risk Analysis of Atrial Fibrillation After Radiotherapy for Breast Cancer: Protocol for the Cross-Sectional Cohort Study “Watch Your Heart (WATCH)”

The required number of patients was set to 200 based on a statistical power of 80% with a type I error rate of 5% and theoretical percentages of AF incidence of 10% for the group of patients considered moderately exposed (75th percentile of the average heart radiation dose distribution) [60]. We plan to include these 200 patients in approximately 30 months.

Laura Saint-Lary, Baptiste Pinel, Loic Panh, Gaelle Jimenez, Julien Geffrelot, Youlia Kirova, Jeremy Camilleri, David Broggio, Marie-Odile Bernier, Corinne Mandin, Christelle Levy, Serge Boveda, Juliette Thariat, Sophie Jacob

JMIR Res Protoc 2025;14:e67875

Transforming Health and Reducing Perinatal Anxiety Through Virtual Engagement: Protocol for a Randomized Controlled Trial

Transforming Health and Reducing Perinatal Anxiety Through Virtual Engagement: Protocol for a Randomized Controlled Trial

Overview of surveys and schedule of data collection for the Transforming Health and Reducing Perinatal Anxiety through Virtual Engagement (THRIVE) phase I randomized clinical trial a Not applicable. b GAD-7: Generalized Anxiety Disorder 7 Scale. c PSS-4: Perceived Stress Scale 4. d PRAS: Pregnancy Related Anxiety Scale. e ISI: Insomnia Severity Index. f PHQ-9: Patient Health Questionnaire-9.

Carolyn Ponting, Rebecca J Baer, Kacie Blackman, Bridgette Blebu, Jennifer N Felder, Scott Oltman, Karen M Tabb, Laura Jelliffe Pawlowski

JMIR Res Protoc 2025;14:e70627