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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01839409
Other study ID # 2011-A001359-32
Secondary ID N° 11P03919 / N°
Status Recruiting
Phase N/A
First received April 22, 2013
Last updated November 2, 2015
Start date April 2013

Study information

Verified date November 2015
Source University Hospital, Caen
Contact Pierre Denise, MD PhD
Phone 33231068214
Email pierre.denise@unicaen.fr
Is FDA regulated No
Health authority France: Agence Nationale de Sécurité du Médicament et des produits de santé
Study type Interventional

Clinical Trial Summary

The purpose of this study is to study the relationship between the vestibular system and chronobiology


Description:

The purpose of this study is to study the relationship between the vestibular system and chronobiology.

Two parts will be performed. In the first one patients with bilateral vestibular areflexia will be compared to control subjects.

In the second the effect of vestibular stimulation on circadian rhythms will be evaluated


Recruitment information / eligibility

Status Recruiting
Enrollment 96
Est. completion date
Est. primary completion date April 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 20 Years and older
Eligibility Inclusion Criteria:

- No treatment changing vigilance/wakefulness

- Moderate caffein uptake (2 to 3 cups a day)

- Moderate smoker (5 cigarettes a day)

- Regular sleeping habits

Exclusion Criteria:

- Sleeping duration <6 hours or >9 hours

- Night workers

- Pregnancy

- Sleep or wakefulness disorders

- Progressive neurodegenerative disorders

- Progressive psychiatric disorders

- Thyroid disease

- Type 1 diabetes

- Not able to practice physical activity

- Drug or alcohol addiction during the last 6 months

Study Design

Allocation: Non-Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Basic Science


Related Conditions & MeSH terms


Intervention

Behavioral:
vestibular stimulation
Physical activity and vestibular stimulation will be used in order to improve circadian rhythms

Locations

Country Name City State
France Umr Ucbn/Inserm U1075 Comete Caen CEDEX Basse-Normandie

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Caen

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Measurements of vestibular reflexes (ocular and spinal) and circadian rhythms of biological functions. Gain of vestibular ocular reflex Amplitude of vestibular spinal reflex Amplitude and phase of temperature circardian rhythms 3 years No