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Clinical Trial Summary

This study is to determine the impact of night shift nurse's activity on patients' sleeping patterns in medical services including individual, clinical and environmental factors. The patients will be questioned in order to create both a control group and a group with troubled sleeping patterns.


Clinical Trial Description

There are 5 speciality medical units involved. Patients must respond to the define inclusion criteria. Each patient will be asked if they agree to participate and if so will be asked to consent to participate.

Every day, nurses will give a questionnaire which will be completed by the patient to know if there were troubles sleeping patterns. If so, a second questionnaire will be completed by the patient.

Other data will be recorded such as personal informations, diagnostic, medical history, consumption habits and treatments.

The inclusion phase lasts 15 days maximum. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03370354
Study type Observational
Source Central Hospital, Nancy, France
Contact Bridey Céline
Phone +33383154081
Email c.bridey@chru-nancy.fr
Status Not yet recruiting
Phase N/A
Start date February 1, 2018
Completion date August 15, 2019

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