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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06027047
Other study ID # ROA101
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date September 1, 2023
Est. completion date January 15, 2024

Study information

Verified date August 2023
Source Raivotech
Contact Emmanouil Bakopoulos, MSc
Phone +306945108313
Email info@raivotech.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Sleep is not simply the absence of wakefulness. Sleep is an active procedure, normally happening every night, and is absolutely vital. Good sleep is essential for our well-being. Survival without food can be further than without sleep. Work time and commuting time seem to affect total sleep time and night bedtime. Social and work obligation can, therefore, suppress sleep time. Sleep deprived individuals may be facing anxiety and depression symptoms. The aim of this study is to investigate the presence of anxiety and depression symptoms among adults with the use of the smartphone application Onar. Onar app will be used to gather information from wearable devices of the users including total sleep time, sleep efficiency, wake after sleep onset time. An established questionnaire (Hospital Anxiety Depression Scale/ HADS) will be used to quantify and detect the presence of anxiety and depression in the study population.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 50
Est. completion date January 15, 2024
Est. primary completion date December 31, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria: - Acceptance of terms of use of the application must be done prior to participation in the study. - Male and female adults aged =18 years old and =60 years old. - Subjects using the application on a daily basis for at least 1 week prior to participation. Exclusion Criteria: - History of alcohol or other substance abuse.

Study Design


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Raivotech

References & Publications (4)

Bixler EO, Vgontzas AN, Lin HM, Calhoun SL, Vela-Bueno A, Kales A. Excessive daytime sleepiness in a general population sample: the role of sleep apnea, age, obesity, diabetes, and depression. J Clin Endocrinol Metab. 2005 Aug;90(8):4510-5. doi: 10.1210/jc.2005-0035. Epub 2005 Jun 7. — View Citation

Horenstein A, Morrison AS, Goldin P, Ten Brink M, Gross JJ, Heimberg RG. Sleep quality and treatment of social anxiety disorder. Anxiety Stress Coping. 2019 Jul;32(4):387-398. doi: 10.1080/10615806.2019.1617854. Epub 2019 May 13. — View Citation

Sforza E, de Saint Hilaire Z, Pelissolo A, Rochat T, Ibanez V. Personality, anxiety and mood traits in patients with sleep-related breathing disorders: effect of reduced daytime alertness. Sleep Med. 2002 Mar;3(2):139-45. doi: 10.1016/s1389-9457(01)00128-9. — View Citation

Snaith RP. The Hospital Anxiety And Depression Scale. Health Qual Life Outcomes. 2003 Aug 1;1:29. doi: 10.1186/1477-7525-1-29. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary To determine the existence of depression and anxiety symptoms in the study population. Comparison of HADS score with population standardized mean value. 2 weeks
Secondary Correlation of depression and anxiety symptoms with Total sleep time (TST). Total sleep time (TST). 2 weeks
Secondary Correlation of depression and anxiety symptoms with Wake after sleep onset time (WASO). Wake after sleep onset time (WASO). 2 weeks
Secondary Correlation of depression and anxiety symptoms with Sleep Onset Latency (SOL). Sleep Onset Latency (SOL). 2 weeks
Secondary Correlation of depression and anxiety symptoms with Epworth Sleepiness Scale (ESS). Epworth Sleepiness Scale (ESS). 2 weeks
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