NCT03318302

Brief Summary

The aims of this survey are to assess the relationships between exposure to screens of digital media devices, sleep patterns, and daily function such as subjective sleepiness and attention abilities in adult Israel population

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
282

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Feb 2017

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 1, 2017

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 30, 2017

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 30, 2017

Completed
4 months until next milestone

First Submitted

Initial submission to the registry

October 14, 2017

Completed
9 days until next milestone

First Posted

Study publicly available on registry

October 23, 2017

Completed
Last Updated

October 23, 2017

Status Verified

October 1, 2017

Enrollment Period

5 months

First QC Date

October 14, 2017

Last Update Submit

October 18, 2017

Conditions

Sleep DisturbanceAttention Deficit

Outcome Measures

Primary Outcomes (4)

  • sleep quality

    score on the PSQI questionnaire

    30 days

  • subjective sleepiness

    score on the KSS questionnaire

    30 days

  • subjective concentration score

    score on the concentration questionnaire

    30 days

  • exposure time to digital screen

    The exposure time to digital screens in minutes

    30 days

Interventions

SurveyOTHER

Survey of the adult population in Israel

Also known as: Survey of the adult population in Israel

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

Adult population of Isrel

You may qualify if:

  • All of the participants were Hebrew-speaking residents of Israel

You may not qualify if:

  • under 18 years old No Hebrew-speaking residents of Israel

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Haifa

Haifa, Israel

Location

MeSH Terms

Conditions

ParasomniasAttention Deficit Disorder with Hyperactivity

Interventions

Surveys and Questionnaires

Condition Hierarchy (Ancestors)

Sleep Wake DisordersNervous System DiseasesMental DisordersAttention Deficit and Disruptive Behavior DisordersNeurodevelopmental Disorders

Intervention Hierarchy (Ancestors)

Data CollectionEpidemiologic MethodsInvestigative TechniquesHealth Care Evaluation MechanismsQuality of Health CareHealth Care Quality, Access, and EvaluationPublic HealthEnvironment and Public Health

Study Officials

  • Lilach Kemer, Dr.

    Assuta Medial Center

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
ECOLOGIC OR COMMUNITY
Time Perspective
OTHER
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Chief Dr.

Study Record Dates

First Submitted

October 14, 2017

First Posted

October 23, 2017

Study Start

February 1, 2017

Primary Completion

June 30, 2017

Study Completion

June 30, 2017

Last Updated

October 23, 2017

Record last verified: 2017-10

Data Sharing

IPD Sharing
Will not share

Locations

IL(1)