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Pill Bottle vs Reminder App

Primary Purpose

Hypertension, Medication Adherence

Status
Not yet recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Medication Reminder App
Sponsored by
Washington University School of Medicine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Hypertension focused on measuring Occupational Therapy, Medication Management

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: currently be prescribed an antihypertensive medication by their doctor have taken antihypertensive medication for the last year be willing to download and use a new app on their phone for the study score a 34 or lower on the Hill Bone compliance scale Exclusion Criteria: need assistance taking their medications have a severe cognitive impairment have a severe visual impairment that prevents them from reading notifications on their phone use a pillbox to take their medications do not use a smart phone or their smart phone does not meet the requirements for the app to be downloaded

Sites / Locations

  • Washington University in St. Louis

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Active Comparator

Arm Label

MEMS Cap Only

Medication Reminder App + MEMS Cap

Arm Description

If the participant is randomized to the control group, they will: receive a brief education session and be handed a flyer about the importance of medication adherence receive a MEMS cap and be given instructions on how to use it with their blood pressure medication

Intervention group that will be shown how to use the mobile phone medication reminder app and be given assistance downloading and setting it up on their personal phone.

Outcomes

Primary Outcome Measures

Medication Event Monitoring System (MEMS) Cap
The Medication Event Monitoring System (MEMS) measures medication adherence over 30 days at home. In this system, an electronic cap will be placed on a bottle assigned to the participant's antihypertensive medication and records each time the medication bottle is opened. All participants will use the electronic monitoring for one antihypertensive medication taken daily.
Exit interview
In the exit interview, participants will be asked qualitative questions about their experiences in the study and using the MEMS cap and medication reminder app. This will support a robust process evaluation to guide intervention improvements, dissemination, and implementation in a diverse sample.

Secondary Outcome Measures

Full Information

First Posted
September 5, 2023
Last Updated
September 11, 2023
Sponsor
Washington University School of Medicine
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1. Study Identification

Unique Protocol Identification Number
NCT06034301
Brief Title
Pill Bottle vs Reminder App
Official Title
Feasibility of Interventions Impacting Medication Adherence
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
September 2023 (Anticipated)
Primary Completion Date
November 2023 (Anticipated)
Study Completion Date
December 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Washington University School of Medicine

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Current medication adherence interventions are minimally effective, which results in higher rates of morbidity and mortality for 45 million US adults who have hypertension and low adherence. This feasibility randomized controlled trial seeks to understand the efficacy of reminders and monitoring in the form of a mobile phone application vs usual care on medication adherence as well as the feasibility of the intervention and study procedures. This study will compare participants who use a mobile phone app that notifies them when to take their medications (intervention group) to participants who do not get assigned the app (control group) for 30 days. Medication adherence will be monitored using a Medication Event Monitoring System (MEMS) cap. Both groups will also receive the usual care, which will include giving participants a pamphlet about taking their medications. The long-term goal of this work is to improve antihypertensive medication adherence and to decrease morbidity and mortality. The objective of this application is to test the efficacy of the app based reminders and feedback. The hypothesis driving this research is that the intervention will be more effective than the usual care. The specific aims are as follows:
Detailed Description
Current medication adherence interventions are minimally effective, which results in higher rates of morbidity and mortality for 45 million US adults who have hypertension and low adherence. This feasibility randomized controlled trial seeks to understand the efficacy of reminders and monitoring in the form of a mobile phone application vs usual care on medication adherence as well as the feasibility of the intervention and study procedures. This study will compare participants who use a mobile phone app that notifies them when to take their medications (intervention group) to participants who do not get assigned the app (control group) for 30 days. Participants will receive an electronic monitoring cap (i.e. a Medication Event Monitoring System (MEMS) cap) to monitor when they take their antihypertensive medications while they are in the study. Both groups will also receive the usual care, which will include giving participants a pamphlet about taking their medications. The long-term goal of this work is to improve antihypertensive medication adherence and to decrease morbidity and mortality. The objective of this application is to test the efficacy of the app based reminders and feedback. The hypothesis driving this research is that the intervention will be more effective than the usual care. The specific aims are as follows: Aim 1. Compare the efficacy of the app based reminders and feedback with usual care for the primary outcome of medication adherence in 40 adults with hypertension and low adherence. Aim 2. Conduct a robust process evaluation to guide intervention improvements, dissemination, and implementation in a diverse sample. The hypothesis will be tested for two specific aims in 40 adults (20 control, 20 intervention) with hypertension and low adherence. For these aims, the study will be conducted as a phase II single-blind, parallel-group, randomized controlled trial with diverse adults with hypertension over 30 days. Participants will answer surveys about their demographics, knowledge about hypertension, and their medication adherence. They will then be randomized and either be given the standard of care or standard of care plus the intervention (app-based reminders and feedback). The intervention includes a brief training session on downloading and using the medication reminder app. Across arms, Participants will track their medication adherence for 30 days using the MEMS cap. After the 30 days, participants will take surveys about their adherence and knowledge about hypertension and have a brief exit interview with a member of the research team to talk about their experience and debrief them about the study.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypertension, Medication Adherence
Keywords
Occupational Therapy, Medication Management

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Feasibility randomized controlled trial
Masking
Participant
Masking Description
The recruitment material and informed consent will make it appear that the effectiveness between an electronic medication cap and a medication adherence app are being compared and that some participants will get the app while others will get the electronic medication bottle. The reality is that all participants will receive an electronic medication bottle.
Allocation
Randomized
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
MEMS Cap Only
Arm Type
No Intervention
Arm Description
If the participant is randomized to the control group, they will: receive a brief education session and be handed a flyer about the importance of medication adherence receive a MEMS cap and be given instructions on how to use it with their blood pressure medication
Arm Title
Medication Reminder App + MEMS Cap
Arm Type
Active Comparator
Arm Description
Intervention group that will be shown how to use the mobile phone medication reminder app and be given assistance downloading and setting it up on their personal phone.
Intervention Type
Device
Intervention Name(s)
Medication Reminder App
Intervention Description
If the participant is randomized to the intervention group, they will: receive a brief education session and be handed a flyer about the importance of medication adherence. get training on how to use the medication reminder app and participant will be given a user guide on how to use the app demonstrate their understanding on an iPad using the teach back method install and set up the medication reminder app on their phone receive a MEMS cap and be given instructions on how to use it with their blood pressure medication. Study team members will use a participant ID to log into the MEMS cap application; no identifiable information will be entered.
Primary Outcome Measure Information:
Title
Medication Event Monitoring System (MEMS) Cap
Description
The Medication Event Monitoring System (MEMS) measures medication adherence over 30 days at home. In this system, an electronic cap will be placed on a bottle assigned to the participant's antihypertensive medication and records each time the medication bottle is opened. All participants will use the electronic monitoring for one antihypertensive medication taken daily.
Time Frame
30 days
Title
Exit interview
Description
In the exit interview, participants will be asked qualitative questions about their experiences in the study and using the MEMS cap and medication reminder app. This will support a robust process evaluation to guide intervention improvements, dissemination, and implementation in a diverse sample.
Time Frame
30 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: currently be prescribed an antihypertensive medication by their doctor have taken antihypertensive medication for the last year be willing to download and use a new app on their phone for the study score a 34 or lower on the Hill Bone compliance scale Exclusion Criteria: need assistance taking their medications have a severe cognitive impairment have a severe visual impairment that prevents them from reading notifications on their phone use a pillbox to take their medications do not use a smart phone or their smart phone does not meet the requirements for the app to be downloaded
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jaclyn Schwartz, PhD
Phone
(314)273-4398
Email
jaclyns@wustl.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Sami Tayeb, MA
Phone
(314)273-4437
Email
samit@wustl.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jaclyn Schwartz, PhD
Organizational Affiliation
Washington University School of Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Washington University in St. Louis
City
Saint Louis
State/Province
Missouri
ZIP/Postal Code
63110
Country
United States
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sami Tayeb, MA
Phone
314-273-4437
Email
samit@wustl.edu
First Name & Middle Initial & Last Name & Degree
Jaclyn Schwartz, PhD

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Individual participant data that underlie the results reported in any publications, after deidentification (text, tables, figures, and appendices).
IPD Sharing Time Frame
Beginning 9 months and ending 36 months following article publication.
IPD Sharing Access Criteria
Researchers who provide a methodologically sound proposal to achieve the aims in the approved proposal.
IPD Sharing URL
https://beckerdms.wustl.edu/
Citations:
PubMed Identifier
29549075
Citation
Ahmed I, Ahmad NS, Ali S, Ali S, George A, Saleem Danish H, Uppal E, Soo J, Mobasheri MH, King D, Cox B, Darzi A. Medication Adherence Apps: Review and Content Analysis. JMIR Mhealth Uhealth. 2018 Mar 16;6(3):e62. doi: 10.2196/mhealth.6432.
Results Reference
background
Citation
Aldeer M., Javanmard M., & Martin R. P. (2018). A review of medication adherence monitoring technologies. Applied System Innovation, 1(2), 2. https://doi: 10.3390/asi1020014.
Results Reference
background
PubMed Identifier
29785096
Citation
Morrissey EC, Casey M, Glynn LG, Walsh JC, Molloy GJ. Smartphone apps for improving medication adherence in hypertension: patients' perspectives. Patient Prefer Adherence. 2018 May 14;12:813-822. doi: 10.2147/PPA.S145647. eCollection 2018.
Results Reference
background
PubMed Identifier
28993388
Citation
Santo K, Chow CK, Thiagalingam A, Rogers K, Chalmers J, Redfern J. MEDication reminder APPs to improve medication adherence in Coronary Heart Disease (MedApp-CHD) Study: a randomised controlled trial protocol. BMJ Open. 2017 Oct 8;7(10):e017540. doi: 10.1136/bmjopen-2017-017540.
Results Reference
background
PubMed Identifier
31167489
Citation
Santo K, Singleton A, Chow CK, Redfern J. Evaluating Reach, Acceptability, Utility, and Engagement with An App-Based Intervention to Improve Medication Adherence in Patients with Coronary Heart Disease in the MedApp-CHD Study: A Mixed-Methods Evaluation. Med Sci (Basel). 2019 Jun 4;7(6):68. doi: 10.3390/medsci7060068.
Results Reference
background
PubMed Identifier
30150326
Citation
Santo K, Singleton A, Rogers K, Thiagalingam A, Chalmers J, Chow CK, Redfern J. Medication reminder applications to improve adherence in coronary heart disease: a randomised clinical trial. Heart. 2019 Feb;105(4):323-329. doi: 10.1136/heartjnl-2018-313479. Epub 2018 Aug 27.
Results Reference
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Pill Bottle vs Reminder App

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