MobileMedMinder: A Networked Aide for Medication Compliances

• Sponsor: University of Maryland, Baltimore (Other)
• Overall Status: Completed
• CT.gov ID: NCT01597583
• Collaborator: Limaging (Other)
• Enrollment: 34
• Location: 1
• Arms: 2
• Duration (Months): 25
• Patients Per Site Per Month: 1.4

Study Details

Study Description

Brief Summary

The main aim of this study is to conduct a randomized control trial to compare MobileMedMinder, a mobile phone based medication reminder software product, with currently accepted and empirically supported methods for increasing medication compliance through reminders and tracking.

Condition or Disease	Intervention/Treatment	Phase
Heart Failure, Congestive	Behavioral: Use of MobileMedMinder	N/A

Study Design

• Study Type: Interventional
• Actual Enrollment: 34 participants
• Allocation: Randomized
• Intervention Model: Parallel Assignment
• Masking: None (Open Label)
• Primary Purpose: Other
• Official Title: MobileMedMinder: A Networked Aide for Medication Compliances
• Study Start Date: Nov 1, 2011
• Actual Primary Completion Date: Dec 1, 2013
• Actual Study Completion Date: Dec 1, 2013

Arms and Interventions

Arm	Intervention/Treatment
Experimental: Use of MobileMedMinder	Behavioral: Use of MobileMedMinder; Use of an intervention to remind patients to take their medications.
No Intervention: Usual care

Outcome Measures

Primary Outcome Measures

1. Compliance [3 months]

   Pill counts will be used to assess compliance

Eligibility Criteria

Criteria

• Ages Eligible for Study: 18 Years and Older
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: No

Inclusion Criteria:

• Taking beta blockers, ACE or ARB, and hydralazine for treatment of HF.

Exclusion Criteria:

• Inability to understand informed consent

• Inability to read and understand English

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	University of Maryland	Baltimore	Maryland	United States	21201

Sponsors and Collaborators

• University of Maryland, Baltimore
• Limaging

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

• Responsible Party: Stephen Gottlieb, Professor, University of Maryland, Baltimore
• ClinicalTrials.gov Identifier: NCT01597583
• Other Study ID Numbers: HP-00051021
• First Posted: May 14, 2012
• Last Update Posted: Mar 9, 2022
• Last Verified: Feb 1, 2022

• Additional relevant MeSH terms: Heart Failure

Study Results

No Results Posted as of Mar 9, 2022