iTAB-CV RCT: Using mHealth to Improve Adherence and Reduce Blood Pressure in Individuals With Hypertension and Bipolar Disorder
Study Details
Study Description
Brief Summary
This proposed 2-stage randomized controlled trial (RCT) will evaluate a personalized patient-centered adherence intervention iTAB-CV + Self-Monitoring (iTAB-CV + SM) vs. Self-Monitoring (SM) alone in poorly adherent hypertensive persons with BD. This practical, technology-facilitated intervention has potential to improve adherence to antihypertensive medication and reduce SBP among high-risk individuals. The intervention is suitable for primary care or mental health settings and has potential for broad scale-up.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
N/A |
Detailed Description
The proposed 5-year project uses a 2-stage randomized controlled trial (RCT) design (Figure 2) to evaluate a brief, practical adherence intervention (iTAB-CV) delivered via interactive text messaging+ Self-Monitoring (SM) compared to SM alone. 200 individuals with BD and HTN who are < 80% adherent with HTN medicine will be enrolled from mental health and primary care settings and the community. The underlying premise is that improving adherence to antihypertensives in BD is likely to be an efficient path to improving health outcomes in a vulnerable population. Findings on the relationship between habit strength, medication attitudes, mood, and adherence in this project will be generalizable to other populations.
The entire observation duration will be 12 months. In stage 1, after consenting and passing screen, participants will receive an automated device (eCAP) to track their use of antihypertensive medication. Participants will use the eCAP for 2 months until completing their baseline assessment. At that time, they will be randomized to either Arm 1 (iTAB-CV + self-monitoring) or Arm 2 (self-monitoring alone). Both interventions will be provided for 2 months with an interim phone/video assessment for adherence. At the end of this 2 month stage, participants will be seen for either a virtual or in-person assessment.
In stage 2, following the 4-month assessment, those in iTAB-CV will be re-randomized to receive either a high intensity (starts off with 1 reminder per day and tapers down to 1 reminder per week over the course of 2 months) or low intensity (1 reminder per week) booster
- self-monitoring compared to self-monitoring alone. Adherence will be assessed by phone/video at 5 months as an interim measurement and a virtual or in-person assessment will occur at 6 months. In stage 3, investigators will follow participants for another 6 months without intervention with 1 interim phone/video assessment and a final virtual or in-person assessment at 12 months.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: iTAB-CV + Self Monitoring Receives iTAB-CV intervention plus self-monitoring (SM), blood pressure home monitoring, eCAP, and weekly mood rating |
Behavioral: iTAB-CV
Individualized Texting for Adherence Building - Cardiovascular (iTAB-CV): a personalized patient-centered text message-based adherence intervention
|
| Active Comparator: Self Monitoring Receives self-monitoring (SM), blood pressure home monitoring, eCAP, and weekly mood rating |
Behavioral: Self-Monitoring
The Self-Monitoring (control) group will monitor their medication adherence, take their blood pressure weekly with a home blood pressure monitor provided by the study after being trained by the study staff, and rate their mood weekly in response to a text reminder.
|
| Experimental: iTAB-CV + Self Monitoring - High Intensity Booster Following the 4-month assessment, subjects in the iTAB-CV group will be re-randomized to receive either a high intensity booster or low intensity booster. Those in the high intensity booster group will start off receiving 1 reminder per day and taper down to 1 reminder per week over 2 months, in addition to self monitoring. |
Behavioral: iTAB-CV
Individualized Texting for Adherence Building - Cardiovascular (iTAB-CV): a personalized patient-centered text message-based adherence intervention
|
| Experimental: iTAB-CV + Self Monitoring - Low Intensity Booster Following the 4-month assessment, subjects in the iTAB-CV group will be re-randomized to receive either a high intensity booster or low intensity booster. Those in the low intensity booster group will receive 1 reminder per week for 2 months, in addition to self monitoring. |
Behavioral: iTAB-CV
Individualized Texting for Adherence Building - Cardiovascular (iTAB-CV): a personalized patient-centered text message-based adherence intervention
|
Outcome Measures
Primary Outcome Measures
- Change in the Tablet Routine Questionnaire (TRQ) [Baseline and Month 4]
The TRQ item is a subject report of the percentage of prescribed medications not taken within the past month.
- Change in systolic blood pressure (SBP) [Baseline and Month 4]
Systolic blood pressure indicates how much pressure your blood is exerting against your artery walls when the heart beats. Higher reading implies more pressure
- Change in Adherence based on the Electronic Monitoring Device (eCAP) [Baseline and Month 4]
Study participants will be given an eCAP device for one of their pill bottles, which will record time/date of bottle opening. eCAP will be used for the antihypertensive medication that the patient missed the most frequently in the past week (in the case of multiple antihypertensive medications missed the same proportion of times, the medication dosed most often will be chosen). A dose will be counted as "taken" if the bottle is opened within six hours of the prescribed time. We will calculate a percent of doses taken by dividing the number of times the bottle is opened by the number of times it should have been opened as per the prescription.
Secondary Outcome Measures
- Change in Montgomery Asberg Rating Scale (MADRS) score [Month 4 and Month 6]
The MADRS measures symptoms of depression. The minimum possible score is 0 and the maximum score is 60. A higher score implies a worse condition.
- Change in engagement with iTAB intervention [Month 4 and Month 6]
Engagement will evaluated using the percentage of texts messages the subject responds to
- Change in Beliefs About Medicines Questionnaire (BMQ) score [Month 4 and Month 6]
The BMQ assess beliefs about medications. Higher scores indicates stronger beliefs about the components of the scale
- Change in Attitude towards Medication Questionnaire (AMSQ) score [Month 4 and Month 6]
The AMSQ comprises 19 items grouped into 7 subscales: general opposition to prophylaxis (4 items), denial of therapeutic effectiveness (2 items), fear of side effects (2 items), difficulty with medication routines (4 items), denial of illness severity (3 items), negative attitudes toward drugs in general (3 items), and lack of information about psychiatric medication (1 item). Higher scores on each subscale represent more negative attitudes toward mood stabilizers.
- Change in Self-efficacy for Medication Taking Behavior (MASES-R) [Month 4 and Month 6]
The MASES-R measures adherence self-efficacy. Higher scores indicate a greater level of self-efficacy.
- Change in Self-Report Habit Index (SRHI) [Month 9 and Month 12]
The SRHI is a measure of habit strength. The minimum score is 12 and the maximum score is 84. A higher score implies stronger habits.
Eligibility Criteria
Criteria
Inclusion Criteria:
-
Age range: from 21 to 80
-
Have a clinical diagnosis of Bipolar Disorder as determined by a standardized diagnostic interview, the Mini-International Neuropsychiatric Interview (MINI)
-
Have elevated systolic blood pressure ≥130 at screening
-
Have received a diagnosis of hypertension per patient self-report at least 6 months prior to enrollment
-
Have been prescribed at least one regularly scheduled antihypertensive medicine for 3 or more months since diagnosis
-
Be poorly adherent (defined as missing 20% or more of medication within either the past week or past month) with prescribed antihypertensive medication
-
Have their own cellular phone in order to receive text messages as part of the intervention
Exclusion Criteria:
-
Unable/unwilling to participate in psychiatric interviews. This will include individuals, who may be too psychotic to participate in interviews/rating scales
-
Unable/unwilling to give written, informed consent to study participation
-
In the interest of patient safety, individuals who are at high immediate risk for suicide will be excluded from study participation. The suicide risk assessment will be informed by standardized assessments of psychiatric symptoms, the Mini-International Neuropsychiatric Interview (MINI), and the Montgomery Asberg Depression Rating Scale (MADRS). Individuals with active suicidal ideation and recent suicide attempt or current intent and plan will be excluded from study participation. Individuals who score a ≥ 5 on item 10 of the MADRS will be considered to be at high risk for suicide, although individuals with MADRS scores lower than 5 could potentially be excluded if either the psychologist or psychiatrist PIs believe that the individual is at high immediate risk for suicide based upon other input or information. In the event that a potential study participant is determined to be at high risk for suicide, that individual will not be enrolled and the study staff will immediately implement procedures for the safety of the individual. Once that individual is no longer at risk, they may be rescreened for possibility enrollment in the study
-
Individuals who are monolingual, non-English speaking will be excluded. Given the proposed sample sizes of the iTAB-CV + SM and SM alone treatment arms in the proposed study, it would not be practical to conduct sub-group analyses. Based upon our BD adherence work and RCT, which drew upon a population similar to the proposed trial, there were no potential subjects who were excluded from the studies due to inability to speak English. Hispanic individuals made up 3.6% of those enrolled
-
Upper arm circumference > 50cm
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Case Western Reserve University | Cleveland | Ohio | United States | 44106 |
Sponsors and Collaborators
- Case Western Reserve University
- National Heart, Lung, and Blood Institute (NHLBI)
- University of California, San Diego
Investigators
- Principal Investigator: Jennifer Levin, PhD, Case Western Reserve University
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- STUDY20200330
- 1R01HL149409-01A1