Skip to main content
OpenTrials
Recruiting

NCT Number: NCT07087353

Efficacy of Remote Monitoring in Patients Treated for Moderate to Severe Major Depressive Episodes

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.

Recruiting

Interested in participating?

Request Info

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

CHU Besançon, Besançon, France

Loading trial locations.

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adults (≥18 years old) meeting ICD-11 criteria for a moderate to severe major depressive episode
  • Access to a personal smartphone and an internet connection, and cognitively able to use it independently

Exclusion criteria

  • Pregnant women
  • Individuals under legal guardianship or conservatorship
  • Ongoing alcohol or drug abuse considered likely to interfere with study participation, as judged by the investigator
  • Psychiatric or physical comorbidities (e.g., severe neurological or cardiovascular conditions) considered likely to interfere with participation or study results, at the discretion of the Principal Investigator

Treatment and study plan

Edra PRO

Device

Remote monitoring software

Primary outcomes

  1. Response rate over a 6-month period.

    Time frame: Month 6

    Difference in response rates (%) between the intervention group and the control group

Secondary outcomes

  1. Safety and absence of defects in Edra PRO over a 6-month period

    Time frame: Month 6

    Analysis of adverse events in both arms and reported device deficiencies in the intervention group

  2. Impact of Edra PRO versus usual care on patients' quality of life

    Time frame: Month 6

    Short Form-36 questionnaire. Ranges from 0 to 100, with higher scores indicating better health-related quality of life.

  3. Medico-economics impact of Edra PRO versus usual care

    Time frame: Month 6

    Analysis of cost of care

Study contacts

Contact information is provided by the study sponsor or research team.

Charles Ferté

CONTACT

[email protected]

Emma Touré Cuq, PharmD

CONTACT

[email protected]

+33646396617

Sponsors and collaborators

Lead sponsor

Resilience

Industry

Registry information

Official study title

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

Important dates

Study start
2025
Primary completion
2027
Study completion
2027
First posted
Jul 28, 2025
Registry last updated
May 1, 2026

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.

Published trials that share one or more normalized conditions with this study.