Mobile Application and Pregnant Patient Knowledge

• Sponsor: University Hospitals Cleveland Medical Center (Other)
• Overall Status: Completed
• CT.gov ID: NCT03452215
• Collaborator: (none)
• Enrollment: 15
• Location: 1
• Arms: 2
• Actual Duration (Months): 8.7
• Patients Per Site Per Month: 1.7

Study Details

Study Description

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	N/A

Study Design

• Study Type: Interventional
• Actual Enrollment: 15 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: Oct 9, 2018
• Actual Primary Completion Date: May 31, 2019
• Actual Study Completion Date: Jun 30, 2019

Arms and Interventions

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

Outcome Measures

Primary Outcome Measures

1. Pregnancy-specific topic/guideline questionnaire [Outcome assessed up to 23 weeks gestation]

   Number of participants who correctly answer

Secondary Outcome Measures

1. Pregnancy-specific questionnaire [Outcome assessed up to 23 weeks gestation]

   Description of general patient population knowledge of pregnancy-specific topics and guidelines.

2. Gestational weight gain quantification [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.

Eligibility Criteria

Criteria

• Ages Eligible for Study: 16 Years and Older
• Sexes Eligible for Study: Female
• Accepts Healthy Volunteers: No

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

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	University Hospitals	Cleveland	Ohio	United States	44106

Sponsors and Collaborators

• University Hospitals Cleveland Medical Center

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

• Responsible Party: Allison Reid, Principal Investigator, University Hospitals Cleveland Medical Center
• ClinicalTrials.gov Identifier: NCT03452215
• Other Study ID Numbers: 01-18-30
• First Posted: Mar 2, 2018
• Last Update Posted: Jun 11, 2020
• Last Verified: Jun 1, 2020

• Individual Participant Data (IPD) Sharing Statement: No
• Plan to Share IPD: No
• Studies a U.S. FDA-regulated Drug Product: No
• Studies a U.S. FDA-regulated Device Product: No
• Keywords provided by Allison Reid, Principal Investigator, University Hospitals Cleveland Medical Center: Pregnancy; Mobile Phone Application

Study Results

No Results Posted as of Jun 11, 2020