NCT06860165Recruiting
Validation of EmoDTx as a Digital Endpoint for Mood Monitoring in Adult Patients Suffering From Unipolar Depression
Validation of EmoDTx as a Digital Endpoint for Mood Monitoring in Adult Patients With Unipolar Depression: An Observational Study Against Standard Depression Assessment Questionnaires
Source: ClinicalTrials.gov · Last updated 22 Jul 2025 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
The aim of this study is to validate the EmoDTx as a digital tool for mood monitoring in adult patients with unipolar depression. The study is prospective, multicenter, and observational, with a single-arm approach. The device studied, EmoDTx, is a mood-monitoring application that analyzes patients' facial expressions to assess their emotional state. The study aims to compare mood scores obtained via EmoDTx with those of standard depression questionnaires (MADRS, PHQ-9, BDI-II, HAMD-17, QIDS-SR16). It will also provide information on how patients feel about the use of passive monitoring software (without the active involvement of the patient) and how the feedback sent to patients can help in their care. Participants who agree to take part in the study, during a selection visit, will be able to: 1. Install the software on a digital interface (smartphone, computer, etc.) and activate or deactivate it whenever they wish during the 8-week follow-up period. 2. Attend scheduled appointments at the center (a first appointment, then a second 4 weeks later, and a final at 8 weeks) to complete a series of questionnaires, be questioned by the doctor, and fill in other questionnaires on their own. 3. At home, answer questionnaires independently, 2 weeks and 6 weeks after the first appointment. 4. The application's feedback will be deactivated during the first 4 weeks and then reactivated during the final 4 weeks. 5. In parallel, an ancillary study will be conducted on 16 patients enrolled in EMC2FR who accepted and performed the video recording of their structured clinical interview following SCID-5-CV at baseline and 4 weeks.
- Status (registry)
- Recruiting
- Study type
- Observational
- Enrollment
- 98 (estimated)
- First submitted
- 11 Feb 2025
- Start date
- 15 Jul 2025
- Primary completion date
- 9 Dec 2025
- Lead sponsor
- Emobot
- Diseases
- Depression
- NCT number
- NCT06860165
What you commit to
- Study type: Observational
- Planned participants: 98
- From 15 Jul 2025 to the primary completion date, 9 Dec 2025
- 2 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Patients who attempted suicide within the previous last 6 months and presenting with suicidal ideations
Other illness
- Patient presenting with bipolar disorders
- Patients with a contra-indication to the device under evaluation:
- Severe depression requiring hospitalization
- Schizophrenic disorders according to DSM 5 classification
- Major neurocognitive disorders according to DSM 5 classification
- Illiteracy
- Subject hospitalized in a healthcare or social institution for reasons other than biomedical research or is deprived of freedom by administrative or judicial decision or is placed under guardianship
Other
- Patients hospitalized
- Patients taking more than 75% of the maximal recommended daily dose of benzodiazepines
- Patients taking more than 75% of the maximal recommended daily dose of antipsychotics
- Patients taking more than 75% of the maximal recommended daily dose of neuroleptics
- Patients who did not respond to 10 different pharmacological treatments
- Patients unable to read, write and understand French
- Patients with no access to a smartphone or a computer with an internet connection
- Patients who refuse to sign the Patient Informed Consent
- Patients already participating in another interventional clinical study
Who the study is looking for
- Outpatients diagnosed with mild to severe unipolar disorder
- Age ≥ 18 years old
- Patients willing and able to participate (i.e willing to use the EmoDTx App and having the necessary technical equipment to use it)
- Patients who read, write and understand French
- Patients having signed the Patient Informed Consent
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (2)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Cabinet médical Sikorav - Chitic - Roux-Pertus Coordinator of this site? Confirm its status | Changé | France | Recruiting |
| Centre Hospitalier Universitaire de Nîmes Coordinator of this site? Confirm its status | Nîmes | France | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.