Smart Phone Medication Adherence Saves Kidneys--SMASK

Hypertension Clinical Trial

Official title:

Smart Phone Medication Adherence Saves Kidneys--SMASK

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02827695
• Other study ID #: Pro00053471
• Status: Completed
• Phase: N/A
• Start date: May 2016
• Est. completion date: August 31, 2020

Study information

• Verified date: October 2020
• Source: Medical University of South Carolina
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Investigators will employ a 2-arm Randomized Controlled Trial (RCT) design with the subject as the unit of randomization and analysis. Kidney transplant recipients having uncontrolled hypertension will be enrolled into a screening phase to measure medication non-adherence. Each subject will use an electronic pill tray for 1 month without any reminder functions activated. Non-adherent subjects who remain uncontrolled will be randomly assigned to SMASK or Standard Care (SC). SC will continue to use the pill tray with reminders turned off and will receive attention control texts with healthy lifestyle information. SMASK will have the reminder functions of the electronic pill tray activated and will receive a Bluetooth blood pressure monitor and an app to collect the data and send to researchers.

Subjects in the second phase will participate in 4 more evaluations at months 1, 3, 6, 12 post randomization. Research staff will measure resting blood pressure and heart rate.

Description:

A randomized RCT will be conducted with kidney transplant patients identified as hypertensive (>129 SBP following KDIGO guidelines) via medical history. Those identified as being nonadherent for 4 weeks during the first month post enrollment (adherence score <0.85) will be eligible to participate in the second phase. Participants in the second phase will be randomly assigned to standard care (SC) + attention control or the mHealth program plus SC.

Following informed written consent, eligible patients will be asked to complete several brief surveys aimed at determining, mood state, perceived stress, self-efficacy assessment, comfort with mHealth devices, perceptions of treatment burden and attitudes towards mhealth. Subjects will have their blood pressure measured and if SBP is >129 they will enter the screening phase. Subjects will be provided a Medication dispensing device system. Subjects will be called the following day to check if there were any problems in filling the Simplemed tray.

The Simplemed has four compartments for each day of the week for potential use. Microelectronic circuitry in each compartment on the tray date stamps the opening of each compartment and removal of the refill tray. These signals are relayed via an internal modem to a server for processing. Data can then be sent directly into the MUSC server that compiles individuals' health data from multiple delivery points. Adherence rate across the first month will be calculated at weekly intervals.

All subjects will return for a visit at the end of their 4 week screening period. Those with an adherence score <0.85 for 4 weeks and whose SBP continues to be >129 will be invited to participate in the second phase of the RCT. Evaluations performed at this visit will include anthropometrics, questionnaires, and resting BP. A Spacelabs ABP monitor will be applied with instructions for wearing the monitor 24 hrs. The subjects will be randomized to SMASK+SC or SC+ attention control groups after the baseline procedures are completed. Those with med adherence score ≥0.85 or who have SBP ≤ 129 will return their pill tray but not proceed into the second phase. Recruitment will end when 80 subjects have successfully transitioned into the second phase (RCT) of the study.

The SC+ attention control group will continue to use Simplemed with reminder functions disabled, they will be sent daily text messages or links to PDF documents or videos containing health information as attention control. The SMASK mhealth intervention group will also receive SC and have the Simplemed reminder functions turned on (blink for ½ hr when medication is due, chime additional ½ hr, then text or email after 1 hour) and receive training in use of the A&D BP monitor. They will be instructed to measure their blood pressure twice daily AM, PM) on at least every third day. Patients will be provided with and shown how to use the smart phone app and activate the app when they record their blood pressure readings.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 80
• Est. completion date: August 31, 2020
• Est. primary completion date: May 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 21 Years and older

Eligibility

Inclusion Criteria:

1. =21 years old;

2. First time recipient of a functioning solitary kidney transplant;

3. Prescribed =3 medications for immunosuppression and HTN;

4. Transplant MD's assent that patient is able to participate;

5. Ability to speak, hear and understand English;

6. Able to take their own BP;

7. Self-administers medications;

8. SBP >129 mmHg at clinic visit(s) in 4 weeks prior, and at initial study evaluation at enrollment;

9. ***Only subjects with adherence score <.85 after 1-month screening and SBP >129 mmHg at baseline will be randomized.

Exclusion Criteria:

1. Failure to meet any inclusion criterion;

2. Ongoing substance abuse (e.g., >21 alcoholic drinks/week);

3. Psychiatric illness requiring treatment beyond antidepressants;

4. Will attempt to become pregnant within the year;

5. Pregnant or nursing women, prisoners, and institutionalized persons.

Related Conditions & MeSH terms

• Hypertension
• Kidney Transplantation
• Medication Adherence

Intervention

Behavioral:
• SMASK
Medication adherence and BP monitoring
• EnhancedSC
Standard care without med reminder functions with healthy lifestyle texts

Locations

Country	Name	City	State
United States	Medical University of South Carolina	Charleston	South Carolina

Sponsors (1)

Lead Sponsor	Collaborator
Medical University of South Carolina

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Medication Adherence	% with electronic monitor-derived adherence scores >.90;	six months
Secondary	Provider adherence to KDIGO guidelines	measured by timing of medication changes	six months
Secondary	Changes in Self-Determination Theory mediators	Survey responses demonstrate increased (e.g., perceived competence and autonomous regulation).	six months
Secondary	BP control	% reaching and sustaining Kidney Disease Improving Global Outcomes (KDIGO) guidelines for BP control (resting and 24-hr BP<130/80 mmHg).	Six months