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NCT Number: NCT07760350

Assessing the Feasibility of the "Heart Care Pairs" Intervention

The researchers will invite 30 patients in primary care who have high blood pressure to participate in this health program with a supportive partner of their choosing (these will be the "participant pairs"). Participant pairs will be invited to complete the Heart Care Pairs health program that will include up to six sessions each including 1) some education on a health habit like physical activity and heart healthy foods, 2) goal setting together, and 3) talk about healthy communication to support one another with heart healthy habits. The researchers will work with participants to address things that get in the way of coming for visits like offering transportation and offering telehealth visits. The researchers are seeing how this program works in real life so participants will be asked to complete as many sessions as they want to and can attend. The researchers will be interested in what participants think about the sessions, if they were satisfied with the visits, and if they would recommend the program to others in their community. The researchers will ask these questions in interviews with participants. The researchers will also ask up to 25 primary care workers about how they view the program as helpful to their work with patients with high blood pressure and whether they would refer more patients to the program in the future.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Department of Family & Community Medicine; University of Alabama at Birmingham

Birmingham, Alabama, 35205, United States

About this study

The overall objective of the present pilot behavioral trial is to assess the feasibility and acceptability of a dyadic CVD risk reduction intervention to be delivered by behavioral health consultants in primary care practices for patients with HTN. In a preliminary investigation prior to this pilot project, the research team has confirmed feasibility of recruitment of dyads from primary care settings, assessed health and social support needs, and interest in an intervention like Heart Care Pairs while making ongoing systematic adaptations to the intervention. The next phase of pilot work outlined in this proposal will assess if the intervention will work in primary care by assessing retention, treatment process, and acceptability.

Aim 1: To determine the feasibility and acceptability of the Heart Care Pairs intervention with N=30 dyads including patients with HTN attending primary care and their chosen supportive partner using a mixed methods single-arm pragmatic trial.

Hyp 1: Heart Care Pairs will be feasible based on dyads attending <70% of intervention sessions, completion of follow-up assessments and interviews, and overall patient- and partner-reported satisfaction with the intervention.

Aim 2: To assess primary care workflow and PCP acceptability of making referrals to a dyadic behavioral health intervention.

Hyp 2: PCPs will agree that they referred patients to the Heart Care Pairs intervention and that the availability of the referral is helpful for their practice.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Diagnosed with hypertension and/or taking blood pressure lowering medications
  • willing to invite a supportive partner to participate for the duration of the study including an enrollment and baseline measurement visit, up to 6 intervention visits, and a post-intervention measurement visit.

Exclusion criteria

  • untreated serious mental illness or cognitive decline that would limit ability to provide informed consent

Treatment and study plan

Dyadic lifestyle intervention for CVD risk reduction

Behavioral

This is a 6-session behavioral intervention delivered in primary care. The 6 educational topics include: 1) DASH diet; 2) Physical activity; 3) Stress management; 4) Healthy sleep habits; 5) Substance cessation (optional); 6) Adherence to medications and lifestyle habits. All sessions will include collaborative goal setting. And each educational topic will be paired with a communication skill: 1) Seeing others' perspectives; 2) Minimize efforts to control; 3) Non-judgmental language; 4) Support movement towards change; 5) Addressing relapse; and 6) Empathetic responding and self-advocacy.

Primary outcomes

  1. Completion of follow-up assessments

    Time frame: Immediately post-intervention

    Number of surveys and interviews completed

  2. Time to complete recruitment

    Time frame: From study start to end of recruitment, an average of 6 months

    Time from posting recruitment materials to enrollment of 30 dyads

  3. Responsiveness to change on survey measures

    Time frame: Baseline to immediately post-intervention - approximately 12 weeks

    Change scores between baseline assessment to follow-up assessment

  4. Attendance to intervention sessions

    Time frame: Baseline to immediately post-intervention - approximately 12 weeks

    Number of sessions attended compared to number of sessions missed

  5. Treatment Satisfaction Questionnaire

    Time frame: Immediately post-intervention

    Participant ratings of satisfaction with the HCPs intervention. 9-items, with responses on a scale from 1-7. Some items assess satisfaction (1=extremely dissatisfied to 7=extremely satisfied), confidence (1=not at all confident, 7=extremely confident, certainty (1=not at all certain, 7=extremely certain), how easy to use/do the intervention was (1=extremely difficult, 7=extremely easy). Mean scores will be calculated for min score=1 and max score of 7. Higher scores indicate greater satisfaction, and lower burden with the intervention.

Secondary outcomes

  1. Health-related quality of life (HRQoL)

    Time frame: Baseline and immediately post-intervention

    1-item self-rated health status (Bullinger, 1996; Dumas, et al, 2020)

  2. Perceived Stress Scale - 10

    Time frame: Baseline and immediately post-intervention

    10-item Perceived Stress Scale (PSS-10; Roberti, et al, 2006). Responses range from 0=Never to 4=Very often. Scores are summed for total perceived stress score ranging from 0-40 with higher scores meaning higher perceived stress.

  3. Smoking status

    Time frame: Baseline and immediately post-intervention

    1-item cigarette smoking status and number cigarettes per day

  4. Patient Health Questionnaire - 9

    Time frame: Baseline and immediately post-intervention

    PHQ-9 depression screen (Kroenke, et al, 2001). Respondents endorse symptoms of depression over the past 2 weeks on a scale from 0=not at all to 3=nearly everyday. Scores are summed for total scores ranging from 0 to 27 with higher scores indicating greater severity of depression symptoms.

  5. Generalized anxiety disorder (GAD)-7

    Time frame: Baseline and immediately pot-intervention

    GAD-7 screen for anxiety symptoms (Spitzer, et al., 2006). Respondents endorse symptoms of anxiety over the past 2 weeks on a scale from 0=not at all to 3=nearly everyday. Scores are summed for total scores ranging from 0 to 21 with higher scores indicating greater severity of anxiety symptoms.

  6. Body mass index

    Time frame: Baseline and immediately post-intervention

    Approximation of body size based on clinic measured height and weight

  7. Mediterranean Eating Pattern Assessment (MEPA)

    Time frame: Baseline and immediately post-intervention

    Brief assessment of heart healthy eating, self-report recall for past week,16 items. Items assess self-reported number of servings per type of food in the past week. Items are scored based on thresholds meeting a mediterranean diet eating pattern (e.g., greater than or equal to 2 servings of vegetables per day). Scores range from 0-16 with higher scores being more adherent to mediterranean diet pattern (more heart healthy diet).

  8. International physical activity questionnaire short form (IPAQ-SF)

    Time frame: Baseline and immediately post-intervention

    Self-reported walking, moderate physical activity, vigorous physical activity, and sedentary time, 7-items (Lee, et al, 2011). Total met minutes are calculated for each activity domain. Walking MET minutes = 3.3*walking days* walking minutes. Moderate MET minutes = 4.0*moderate days*moderate minutes. Vigorous MET minutes=8.0*vigorous days*vigorous minutes. Total MET minutes = Waling MET min+Moderate MET min+Vigorous MET min.

  9. Sleep time

    Time frame: Baseline and immediately post-intervention

    1-item total average sleep time (Lloyd-Jones, et al, 2022)

  10. Adherence self-report questionnaire (ASRQ)

    Time frame: Baseline and immediately post-intervention

    Self reported medication adherence to blood pressure medicines (Zeller, et al., 2008) 1-item with 1=take all BP medications at the same time every day (excellent adherence) to 6=Hardly take any BP medications (poor adherence).

  11. Treatment Self Regulation Questionnaire

    Time frame: Baseline and immediately post-intervention

    Measure of autonomy, self-report 19-tems (Levesque, et al, 2007). 19-items assessed using a Likert-type scale from 1=Not at all true to 7=Very true. Mean of scores will be calculated with higher score meaning greater autonomy over heart healthy behaviors (taking medications, healthy diet, exercise).

  12. Important other climate questionnaire

    Time frame: Baseline and immediately post-intervention

    Measure of autonomy support, self-report 6-items (Williams, 2006). Responses are on a Likert Scale. Mean scores will be calculated with higher scores indicating greater support from "important others" with efforts to lower blood pressure.

  13. Social Support for Diet and Exercise Behaviors

    Time frame: Baseline and immediately post-intervention

    Social support from family, friends, supportive other related to healthy diet and exercise behavior (Sallis, et al., 1987). Responses range from 0=Rarely to 3=very often. Each question will be asked for "Family," "Friends," and "Study Partner." Mean scores for each relationship type will be calculated with higher scores indicate greater support with health behavior.

  14. Medical Outcomes Study (MOS) Social Support Survey

    Time frame: Baseline and immediately post-intervention

    A total of 19-items self-report for measures of global social support and subscales for: emotional/informational, tangible, affectionate, and positive social interaction. Responses to items range from 1=none of the time to 5=all of the time. The mean items responses are taken for each subscale with higher scores meaning greater social support (Sherbourne & Stewart, 1991)

Sponsors and collaborators

Lead sponsor

University of Alabama at Birmingham

Other

Collaborators

  • National Institute on Minority Health and Health Disparities (NIMHD)

Registry information

Official study title

A Mixed Methods Pilot Feasibility Study of a Primary Care-based Dyadic Cardiovascular Risk Reduction Intervention: "Heart Care Pairs"

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Aug 12, 2026
Registry last updated
Aug 12, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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