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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04703972
Other study ID # 38RC20.087
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date January 13, 2021
Est. completion date June 30, 2022

Study information

Verified date May 2020
Source University Hospital, Grenoble
Contact Mircea POLOSAN, MD-PhD
Phone 04 76 76 54 11
Email MPolosan@chu-grenoble.fr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Relapses in bipolar disorders are associated with a significant proportional functional impact, as well as worsening of the course of bipolar disorder, with impairment of the quality of functional remission, as well as the development of addictive, anxiety and suicidal comorbidities.The functional deficit and the instability of the mood disorder increase with thymic relapses. Currently, these relapses (transition from the state of remission, to a depressive or hyperthymic state) are difficult to predict and to treat because of the absence of correlation between the degree of severity of the stressful event (intensity associated stress) and the occurrence of relapse, taking into account the mediation of this relationship by the stress compensation / adaptation capacities, which are very individual. This project proposes to develop tools based on artificial intelligence technologies to monitor the level of stress and adaptation to life events as well as identifying relapse predictive factors of a patient by using portable and connected devices recording different physiological signals in order to alert him/her when there is a risk of relapse, thus anticipating therapeutic strategies.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 10
Est. completion date June 30, 2022
Est. primary completion date January 31, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria: - Voluntary subjects responding to the diagnosis of bipolar I or II disorder according to the criteria of the DSM-5 - Agreement to benefit from connected objects required for study and able to understand their use - Age between 18 and75 years old - Affiliated to the Social Security system (beneficiary or entitled) - No opposition signed Exclusion Criteria: - Subject included in clinical and/or therapeutic experimentation with exclusion period - Primary psychiatric pathology other than bipolar type I or II disorder - Patient hospitalized without consent - Subject deprived of liberty by judicial or administrative decision - Pregnant, parturient, breastfeeding woman - Known allergy to one of the materials of the bracelets

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
clinical assessment (mood relapses identification)
clinical assessment via psychometric scales physiological data acquired automatically via the connected device (wristwatch, wristband)

Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
University Hospital, Grenoble Commissariat A L'energie Atomique

Outcome

Type Measure Description Time frame Safety issue
Primary Prediction of mood relapses number of relapses predicted by machine learning algorithms versus number of relapses highlighted by clinical assessment at Month 6 of the follow-up
Secondary Correlation between values of Heart rate variability and the occurrence of a thymic relapse (number of relapses during the follow-up period). Heart rate variability (HRV) (ms) at Month 6 of the follow-up
Secondary Correlation between values of skin surface temperature and the occurrence of a thymic relapse (number of relapses during the follow-up period). Physical parameters measured: Skin surface temperature in °C at Month 6 of the follow-up
Secondary Correlation between values of actimetry and the occurrence of a thymic relapse (number of relapses during the follow-up period). Physical parameters measured: Actimetry using accelerometer (movement per minute) at Month 6 of the follow-up
Secondary Correlation between ElectroDermal activity and the occurrence of a thymic relapse (number of relapses during the follow-up period). ElectroDermal activity (siemens) at Month 6 of the follow-up
Secondary Correlation between sleep periods and the occurrence of a thymic relapse (number of relapses during the follow-up period). Sleep periods at Month 6 of the follow-up
Secondary Correlation between social measures and the occurrence of a thymic relapse (number of relapses during the follow-up period). The internet connection times (minute), including social networks, the number and duration (minute) of telephone calls and the number and length (number of characters) of text messages will be automatically recorded daily in order to provide parameters that help quantify the patient's social activity. at Month 6 of the follow-up
Secondary Correlation between values of clinical characteristics (age of onset) and the occurrence of a thymic relapse (number of relapses during the follow-up period). Age of onset (in years) at Month 6 of the follow-up
Secondary Correlation between values of clinical characteristics about thyme episode and the occurrence of a thymic relapse (number of relapses during the follow-up period). Predominant polarity (hypo/manic or depressive or without), polarity of last episode (hypo/manic or depressive), number of previous thymic episodes, duration of remission (in month). at Month 6 of the follow-up
Secondary Correlation between values of clinical characteristics (suicide attempts) and the occurrence of a thymic relapse (number of relapses during the follow-up period). Number of suicide attempts. at Month 6 of the follow-up
Secondary Correlation between values of clinical characteristics (hospitalizations) and the occurrence of a thymic relapse (number of relapses during the follow-up period). Number of hospitalizations. at Month 6 of the follow-up
Secondary Correlation between values of clinical characteristics (comorbid disorders) and the occurrence of a thymic relapse (number of relapses during the follow-up period). History and presence of comorbid disorders. at Month 6 of the follow-up
Secondary Correlation between values of clinical characteristics (medication) and the occurrence of a thymic relapse (number of relapses during the follow-up period). Medication load (in Chlorpromazine equivalent for antipsychotic medication, Chen&Davis). at Month 6 of the follow-up
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