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Promoting Medication Adherence Among Older Adults With Hypertension

Overcoming Immunity to Change: A Feasibility Study of a New Method to Promote Medication Adherence Among Older Adults With Hypertension

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02846220
Enrollment
36
Registered
2016-07-27
Start date
2016-10-31
Completion date
2019-12-30
Last updated
2020-10-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypertension

Keywords

Medication Adherence, Middle Aged 45-64, Aged 65-79, Aged, 80 and over

Brief summary

Over 70% of US adults 65 or older are diagnosed with hypertension, the leading cause of cardiovascular disease and premature deaths in the world. Despite availability of effective drugs to control blood pressure, uncontrolled blood pressure and low adherence to antihypertensive drugs persist as major public health and clinical challenges. On average, 50% of adults adhere to chronic disease medications and lower levels of adherence are associated with worse blood pressure control and adverse outcomes. Many barriers to adherence are well known and have been targeted in interventions to improve medication adherence. As of yet, no single intervention has emerged as superior or even particularly effective in improving adherence. The investigators have recently identified unconscious, self-protective 'hidden motives' that contribute to nonadherence to chronic disease medications. There is a critical need to expand on this insight to test the potential for targeting individuals' 'hidden motives' for low adherence using an innovative learning process called Immunity-to-Change. As a critical step in testing this intervention to target these 'hidden motives', the investigators will undertake a pilot study to assess the feasibility and acceptability of the Overcoming Immunity-to-Change intervention and determine effect sizes of the intervention on adherence, blood pressure (BP) control, and quality of life (QOL). The investigators will test the Immunity-to-Change intervention in a sample of nonadherent older adults with hypertension (n=18). Another sample of nonadherent older adults with hypertension will be monitored for comparison (n=18).

Interventions

BEHAVIORALOvercoming Immunity to Change health coaching

Sponsors

Minds at Work
CollaboratorUNKNOWN
Ohio State University
CollaboratorOTHER
Tulane University School of Medicine
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
55 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Men and women ages 55 and older, with the goal of a sex- and race-balanced sample * Diagnosis of essential hypertension * Uncontrolled hypertension * Current treatment with antihypertensive medication * Low antihypertensive pharmacy refill * English speaking * Telephone access * Ability to read print on a computer screen and use the computer keyboard * Written consent to participate and HIPAA authorization * Written acceptance of study contract * Approval of health care provider

Exclusion criteria

* Cognitive impairment * Enrollment in another clinical trial

Design outcomes

Primary

MeasureTime frameDescription
Change in medication adherence (PDC)Baseline to 6 monthsChange in proportion of days covered (PDC) from baseline to 6 months

Secondary

MeasureTime frameDescription
Change in proportion with low adherence (KWood-4)Baseline to 6 monthsChange in proportion with low adherence (KWood-4\>0) from baseline to 6 months
Change in medication adherence (MMAS-8)Baseline to 6 monthsChange in MMAS-8 score from baseline to 6 months
Change in medication adherence (KWood-4)Baseline to 6 monthsChange in KWood-4 score from baseline to 6 months
Change in proportion with low adherence (PDC)Baseline to 6 monthsChange in proportion with low adherence (PDC\<0.8) from baseline to 6 months
Change in proportion with low adherence (MMAS-8)Baseline to 6 monthsChange in proportion with low adherence (MMAS-8\<6) from baseline to 6 months
Change in diastolic blood pressureBaseline to 6 monthsChange in diastolic blood pressure from baseline to 6 months
Change in proportion with controlled blood pressureBaseline to 6 monthsChange in proportion with controlled blood pressure (SBP\<140 & DBP\<90) from baseline to 6 months
Change in health-related quality of lifeBaseline to 6 monthsChange in health-related quality of life score (SF-36) from baseline to 6 months
Change in systolic blood pressureBaseline to 6 monthsChange in systolic blood pressure from baseline to 6 months

Other

MeasureTime frameDescription
Change in self-efficacy (MUSE)Baseline to 6 monthsChange in score on MUSE scale from baseline to 6 months
Change in self-efficacy (Self-Efficacy for Managing Chronic Disease)Baseline to 6 monthsChange in score on SEMCD scale from baseline to 6 months
Change in hidden motives scoreBaseline to 6 monthsChange in hidden motives score from baseline to 6 months
Change in perceived stressBaseline to 6 monthsChange in score on 4-item version of Perceived Stress Scale from baseline to 6 months
Change in chronic stressBaseline to 6 monthsChange in chronic stress from baseline to 6 months, as measured by salivary cortisol
Change in explicit attitudes scoreBaseline to 6 monthsChange in explicit attitudes score (Beliefs about Medicines Questionnaire) from baseline to 6 months
Change in implicit attitudes scoreBaseline to 6 monthsChange in implicit attitudes score (d-score from single-category implicit association test) from baseline to 6 months
Change in explicit ambivalence scoreBaseline to 6 monthsChange in explicit ambivalence score (absolute value of difference between standardized positive and negative explicit attitudes scores) from baseline to 6 months
Change in implicit ambivalence scoreBaseline to 6 monthsChange in implicit ambivalence score (absolute value of difference between standardized explicit and implicit attitude scores)
Change in short risk aversion switch pointBaseline to 6 monthsChange in short switch point on risk aversion scale from baseline to 6 months
Change in long risk aversion switch pointBaseline to 6 monthsChange in long switch point on risk aversion scale from baseline to 6 months
Change in risk valuationBaseline to 6 monthsChange in value indicated on risk aversion scale from baseline to 6 months
Change in medication-taking self-efficacy (MUSE)Baseline to 6 monthsChange in score on MUSE medication-taking subscale from baseline to 6 months
Change in learning-about-medications self-efficacy (MUSE)Baseline to 6 monthsChange in score on MUSE learning-about-medications subscale from baseline to 6 months

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026