Edra PRO
DeviceRemote monitoring software
NCT Number: NCT07087353
Mood disorders like depression and bipolar disorder are widespread and cause serious psychological, cognitive, and social impairments, with a high burden on healthcare systems. Edra PRO is a digital medical device developed to support clinical decision-making and remotely monitor symptoms in psychiatric patients. The EC-102 randomized controlled trial will evaluate its impact compared to usual care on symptoms, quality of life, healthcare costs, comorbidities, and user adherence and satisfaction.
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Not applicable
CHU Besançon, Besançon, France
Mood disorders such as depression and bipolar disorder affect a large portion of the global population and cause significant psychological, cognitive, and functional impairments, along with high healthcare costs. Despite available treatments, sustained remission is hard to achieve, and many patients experience persistent symptoms and treatment side effects. Continuous remote monitoring could improve care and outcomes. Edra PRO is a digital medical device designed for remote symptom tracking and clinical decision support in psychiatry. The EC-102 randomized controlled trial will assess the impact of Edra PRO versus usual care on symptoms, quality of life, healthcare costs, comorbidities, and user satisfaction and adherence.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Remote monitoring software
Time frame: Month 6
Difference in response rates (%) between the intervention group and the control group
Time frame: Month 6
Analysis of adverse events in both arms and reported device deficiencies in the intervention group
Time frame: Month 6
Short Form-36 questionnaire. Ranges from 0 to 100, with higher scores indicating better health-related quality of life.
Time frame: Month 6
Analysis of cost of care
Contact information is provided by the study sponsor or research team.
Charles Ferté
CONTACT
Emma Touré Cuq, PharmD
CONTACT
Resilience
Industry
A Randomized Controlled Trial Assessing the Efficacy of Remote Patient Monitoring in Patients Treated for a Moderate to Severe Major Depressive Episode
Acronym: EC-102
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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