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Study identifier: NCT06837311 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Post-Stroke Secondary Prevention With Digital Monitoring

Condition: Stroke  ·  Sponsor: University Hospital, Bordeaux

PhaseNA
Planned participants388
Who can joinAll sexes, 18 Years to 80 Years
Healthy volunteersNo

About this study

Stroke is the second leading cause of death and a major cause of disability worldwide. In 2019, Disability-Adjusted Life-Years (DALYs) related to stroke was estimated to have reached 143 million. Modifiable stroke risk-factors, which include poor lifestyle habits (tobacco, alcohol and illicit drug abuse, dietary patterns at risk, low physical activity), account for 90 % of the risk of stroke. Stroke complications and the risk of stroke recurrence is highly dependent on the control of these risk factors. Thus, the secondary prevention of stroke requires profound lifestyle modifications including substance use cessation and diet changes. National guidelines for stroke clinical practice advocate an immediate cessation of consumption of all substances but without recommendations on specific therapeutic regimens. Moreover, none address the management of poor coping with stress or mood problems though they are major population attributable risk factors of stroke and constitute major barriers of behavior changes achievement. Yet, post-stroke emotional impairments are frequent, post-stroke depression and anxiety being the most frequent (prevalence is 30% and 25%, respectively). Importantly, independently from stroke, emotional impairments or disorders and Substance Related and Addiction Disorders (SRADs) are frequent comorbid conditions (dual disorders) with debilitating consequences and the interplay between the two conditions makes rehabilitation more complex. This suggests that ta…

This description comes directly from the study's public registry record.

Talk to the study team

Igor SIBON  ·  0556795520  ·  igor.sibon@chu-bordeaux.fr

Sylvie BERTHOZ  ·  sylvie.berthoz-landron@inserm.fr

Always discuss trial participation with your own doctor first.

Locations (1)

CHU de BordeauxBordeaux, FranceRecruiting

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Source record: clinicaltrials.gov/study/NCT06837311