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Mobile Application and Pregnant Patient Knowledge

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ClinicalTrials.gov Identifier: NCT03452215
Recruitment Status : Recruiting
First Posted : March 2, 2018
Last Update Posted : October 11, 2018
Sponsor:
Information provided by (Responsible Party):
Allison Reid, University Hospitals Cleveland Medical Center

Brief Summary:
Randomized controlled trial to investigate the impact of a pregnancy-specific mobile phone application on the knowledge of specific pregnancy topics and guidelines.

Condition or disease Intervention/treatment Phase
Pregnancy Mobile Application Behavioral: Mobile Phone Application Educational Resources Behavioral: Mobile Phone Application GWG Tracker Not Applicable

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 230 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Prevention
Official Title: Impact of Mobile Application on Patient Knowledge of Pregnancy Topics
Actual Study Start Date : October 9, 2018
Estimated Primary Completion Date : May 31, 2019
Estimated Study Completion Date : June 30, 2019

Arm Intervention/treatment
Experimental: Study Behavioral: Mobile Phone Application Educational Resources
Mobile Phone Application Educational Resources

Behavioral: Mobile Phone Application GWG Tracker
Mobile Phone Application GWG Tracker

Sham Comparator: Control Behavioral: Mobile Phone Application Educational Resources
Mobile Phone Application Educational Resources




Primary Outcome Measures :
  1. Pregnancy-specific topic/guideline questionnaire [ Time Frame: Outcome assessed up to 23 weeks gestation ]
    Number of participants who correctly answer


Secondary Outcome Measures :
  1. Pregnancy-specific questionnaire [ Time Frame: Outcome assessed up to 23 weeks gestation ]
    Description of general patient population knowledge of pregnancy-specific topics and guidelines.

  2. Gestational weight gain quantification [ Time Frame: Outcome assessed through study completion, an average of 7 months ]
    Quantify total gestational weight gain with and without intervention from final documented weight during pregnancy.



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Ages Eligible for Study:   16 Years and older   (Child, Adult, Older Adult)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • 18 years of age or older at time of consent (or 16-17 years of age with guardian present)
  • Singleton gestation

Exclusion Criteria:

  • Inadequate knowledge of English language
  • Inability to read at or above 8th grade level
  • Prior diagnosis of eating disorder

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03452215


Contacts
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Contact: Allison Reid, BS 216-844-8545 Allison.Reid@UHhospitals.org

Locations
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United States, Ohio
University Hospitals Recruiting
Cleveland, Ohio, United States, 44106
Contact: Allison Reid         
Sponsors and Collaborators
University Hospitals Cleveland Medical Center

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Responsible Party: Allison Reid, Principal Investigator, University Hospitals Cleveland Medical Center
ClinicalTrials.gov Identifier: NCT03452215     History of Changes
Other Study ID Numbers: 01-18-30
First Posted: March 2, 2018    Key Record Dates
Last Update Posted: October 11, 2018
Last Verified: October 2018
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No

Keywords provided by Allison Reid, University Hospitals Cleveland Medical Center:
Pregnancy
Mobile Phone Application