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N/A Completed N=1,592 Randomized Single-blind Treatment

Southeastern Collaboration to Improve Blood Pressure Control

Source: ClinicalTrials.gov NCT02866669 ↗
Enrolled (actual)
1,592
Serious AEs
51.5%
Results posted
Oct 2023
Primary outcomePrimary: Number of Participants With Blood Pressure Control (Systolic Pressure Less Than 140 mm Hg and Diastolic Pressure Less Than 90 mm Hg) at 12 Months — 112; 87; 130; 92 participants

Summary

The central objective of this proposal is to rigorously compare two strategies designed to improve BP control in primary care practices serving rural Southeastern African Americans with low socioeconomic status (SES) living in the "Black Belt". In year 1, we're engaging community members (community members who have experience being community peer advisors or have high blood pressure) to develop the study interventions and protocols. In years 2-5, the investigators will test the interventions. Year 2-5, Aim 3: Enroll 80 practices and 25 African American patients with uncontrolled HTN at each practice (total n=2000) in a cluster-randomized, controlled, 4-arm pragmatic implementation trial to evaluate the three multi- component, multi-level functional interventions finalized in the UH2 phase compared with enhanced usual care. The study's 4 arms are: 1. Enhanced Usual Care: Practices are provided with educational materials and tools to enhance patient care 2. Peer Coaching: Patients enrolled in these practices will be matched with a peer coach. The peer coach helps the patient to set goals around self-management, including medications, home monitoring, and diet and exercise, and she helps the patient to strategize how to accomplish the goals, using motivational interviewing techniques 3. Practice Facilitation: Practices randomized to this arm will work with a practice facilitator. Practice facilitation is a highly customized, staged approach to helping a practice to implement process and structural changes to enhance the quality of care and improve patient and staff satisfaction 4. Peer coaching and practice facilitation: Practices randomized to this arm will receive both the peer coach intervention and the practice facilitation intervention. Practice facilitators and peer coaches will receive the same training for this hybrid intervention, but the practice facilitator change packet will add examples of activities that integrate peer coaches.

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Participants With Blood Pressure Control (Systolic Pressure Less Than 140 mm Hg and Diastolic Pressure Less Than 90 mm Hg) at 12 Months
112; 87; 130; 92
SECONDARY
Change in Systolic Blood Pressure Between Baseline and 12 Months
-11; -10; -11; -12
SECONDARY
Change in Satisfaction With Chronic Illness Care Between Baseline and 12 Months
0; 0; 0; 0
SECONDARY
Change in Physical Component Summary Score (PCS) of the Short Form 12 (SF12)
2; 1; 2; 2
SECONDARY
Change in the Mental Component Summary Score (MCS) From the Short Form 12 (SF12)
3; 2; 3; 3
SECONDARY
Self-reported ED Visit or Evidence of an ED Visit at Chart Review Between Baseline and 6 Months
90; 53; 77; 65
SECONDARY
Self-reported ED Visit or Evidence of an ED Visit in Chart Review Between 6 Months and 12 Months
78; 59; 66; 55
SECONDARY
Self-reported Hospitalization or Evidence of Hospitalization in Chart Review Between Baseline and 6 Months
32; 29; 32; 28
SECONDARY
Self-Reported Hospitalization or Evidence of Hospitalization in Chart Review Between 6 Month and 12 Month
24; 35; 32; 30
SECONDARY
Change in Perceived Stress
0; -1; -1; -1

Eligibility Criteria

Inclusion Criteria

  • African American adults aged 19-85 years
  • Uncontrolled HTN, defined as BP >140/90 mm Hg at the time of study enrollment
  • Black Belt resident
  • English speaking
  • Willing to work with a peer coach
  • Willing to sign informed consent

Exclusion Criteria

  • Plans to move out of the area within the next two years
  • Advanced illness with limited life expectancy
  • Pregnant or plans to get pregnant in the next year
  • Advanced chronic kidney disease (estimated glomerular filtration rate <45 ml/min/1.73 m2)
  • Unwillingness to work with a peer coach or to sign informed consent
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02866669). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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