Digital Intervention Participation in DASH
Optimizing Inclusion of Blacks Within a Dietary Change Intervention to Reduce Hypertension
2 other identifiers
observational
30
1 country
1
Brief Summary
This study will examine the context of making high quality dietary choices among Black adults with hypertension. Secondly, this study will also investigate what Black adults need or desire to participate in a digital intervention to improve dietary quality by adopting the DASH eating pattern.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for all trials
Started Sep 2020
Typical duration for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
August 12, 2020
CompletedFirst Posted
Study publicly available on registry
August 17, 2020
CompletedStudy Start
First participant enrolled
September 9, 2020
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 31, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
March 31, 2023
CompletedApril 27, 2021
April 1, 2021
2.6 years
August 12, 2020
April 23, 2021
Conditions
Outcome Measures
Primary Outcomes (1)
Barriers and facilitators of recruitment
Using individual interviews to elicit information of potential recruitment preferences
day 1
Secondary Outcomes (2)
Barriers and facilitators of diet quality
day 1
Comparison of recruitment methods
Baseline
Interventions
A qualitative examination of barriers and facilitators of the DASH dietary pattern, and quantitative investigation of the types of recruitment methods effective for black adults entering a digital DASH-promoting intervention.
Eligibility Criteria
Community sample
You may qualify if:
- self-identify as having high blood pressure
- self-identify as Black/African American/Afro-Caribbean
- at least 18 years old
- self-reported body mass index≥ 18.5 kg/m2
- email address
- English is primary language
You may not qualify if:
- planning to leave the area during study time period
- participating in a related trial
- cardiovascular disease event (e.g. stroke, myocardial infarction) in prior 6 months
- pregnancy - current or planned during the study period
- active malignancy
- recent psychiatric institutionalization
- documented dementia
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University of Connecticutlead
- Duke Universitycollaborator
- National Heart, Lung, and Blood Institute (NHLBI)collaborator
Study Sites (1)
University of Connecticut
Storrs, Connecticut, 06103, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Loneke Blackman Carr, PhD, RD
University of Connecticut
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor
Study Record Dates
First Submitted
August 12, 2020
First Posted
August 17, 2020
Study Start
September 9, 2020
Primary Completion
March 31, 2023
Study Completion
March 31, 2023
Last Updated
April 27, 2021
Record last verified: 2021-04
Data Sharing
- IPD Sharing
- Will not share