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OpenTrials
Completed

NCT Number: NCT03167346

The Investigation of Public Awareness of Core Stroke Symptoms

To investigate public awareness of core stroke symptoms in more than 40 years old population and its related factors.

Completed

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Key information

Age range

40 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Department of Neurology,Peking Union Medical College Hospital,Shuaifuyuan 1,Dong Cheng District. Beijing

Beijing, Beijing Municipality, 100730, China

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • More than 40 years old (born before December 31st 1976) without specific requirements.
  • Be able to finish the questionnaire.

Exclusion criteria

  • Participants with disturbance of consciousness.

Treatment and study plan

Primary outcomes

  1. awareness rate

    Time frame: 2017-2017

    The awareness rate of core symptoms (FAST: facial droop, arm weakness, speech disturbance, time to call an ambulance)

Secondary outcomes

  1. Associated factors

    Time frame: 2017-2017

    The associated factors with the stroke recognition/ correct action to stroke

  2. Subgroup analysis

    Time frame: 2017-2020

    Analysis of stroke recognition rate and correct action rate and their associated factor in subgroups.

Sponsors and collaborators

Lead sponsor

Peking Union Medical College Hospital

Other

Registry information

Acronym: IPACSS

Important dates

Study start
2017
Primary completion
2017
Study completion
2021
First posted
May 25, 2017
Registry last updated
Oct 8, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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