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Sleep Disorders in Transient Ischemic Attack and Stroke: SOMN'AIC Study

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Civil Hospices of Lyon

Status

Completed

Conditions

Stroke
Sleep Disorder

Treatments

Other: Questionnaires

Study type

Observational

Funder types

Other

Identifiers

NCT03274505
69HCL17_0418

Details and patient eligibility

About

Sleep disorders in the setting of stroke are numerous, including sleep-related breathing disorders, insomnia, excessive daytime sleepiness and restless legs syndrome. Consequences of theses sleep disturbances include impaired functional outcome and quality of life, anxious and depressive troubles and increased cardio-vascular morbi-mortality. Mechanisms underlying sleep disorders in the setting of stroke are complex and still partly elucidated. They probably involve the consequences of the ischemic lesion and of the handicap, but also of associated vascular risk factors and more generally pre-existent medical history, or they could represent themselves a risk factor for stroke. Transient ischemic attack (TIA) is a particular condition in which risk factors and background of patients are similar to that observed in stroke, without any cerebral lesion and no persistent neurological deficit. The main objective of the SOMN'AIC study is to compare the prevalence of sleep disorders in stroke and in transient ischemic attack (TIA). The study hypothesis is that the prevalence of sleep disorders may be higher in stroke than in TIA patients, reflecting the consequences of the lesion and the associated handicap.

Enrollment

153 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Stroke group: patients with a diagnosis of stoke and seen at the routine post-stroke 3 month' rehabilitation examination
  • TIA group: diagnosis of a TIA by a stroke specialist at the "SOS TIA" examination
  • > 18 years

Exclusion criteria

  • Refusal to participate
  • Severe cognitive impairment leading to inability to fulfil questionnaires
  • For the TIA group: presence of an ischemic lesion on CT scan or MRI

Trial design

153 participants in 2 patient groups

Stroke patients
Description:
Patients seen by a rehabilitation physician at a routine 3 months' post-stroke examination
Treatment:
Other: Questionnaires
TIA patients
Description:
Patients seen by a stroke specialist at the "SOS TIA" examination
Treatment:
Other: Questionnaires

Trial contacts and locations

3

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Central trial contact

Laure PETER-DEREX, MD, PhD

Data sourced from clinicaltrials.gov

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