The BASIC-S Feasibility Study for Vascular Risk Reduction (NCT07755631)
Piloting an Integrated Lifestyle Intervention for Vascular Risk Reduction: The BASIC-S Feasibility Study
๐ฉบ Plain-English Summary (8th-Grade Level)
Vascular risk factors drive stroke, heart disease, and dementia, but translating lifestyle guidelines into routine clinical care remains challenging. To address this, we developed BASIC-S (Blood Pressure, Activity, Sleep, Interaction, Consumption, and Support), a framework targeting Blood pressure, Activity, Sleep, Interaction (socially), Consumption (nutrition), and Support using partner support and motivational interviewing. This individual-focused approach bypasses the logistical and financial barriers of complex clinical interventions by using sustained behavioral science to support gradual lifestyle changes. This study is a single-center, mixed-methods, cluster-randomized pilot trial evaluating the feasibility of the BASIC-S protocol in an occupational setting. A maximum of 60 households (120 participants) will be randomized 1:1 to either the BASIC-S intervention (motivational coaching, secure video check-ins, automated text messages, and a digital workbook) or standard care. Outcomes will assess feasibility, acceptability, and the validity of new tracking metrics to inform a future full-scale trial.
Who can join: Review the eligibility criteria below.
Location: London Health Sciences Centre (LHSC) โ London, Ontario
Age range: 18 Years
๐งช Interventions in This Study
- BASIC-S Intervention (BEHAVIORAL)
- Standard / Usual Care (BEHAVIORAL)
๐ "Do I Qualify?" โ 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria โ
๐ All Participating Trial Locations (1 Sites)
- London Health Sciences Centre (LHSC) โ London, Ontario
๐ Contact the Study Coordinator
Phone: (519) 685-8500
Email: andrew.appleton@lhsc.on.ca
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
๐ฐ Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in Hypertension (HTN)
- Mediterranean-DASH Intervention for Neurodegenerative Delay and High-Intensity Interval Training in Adults With Hypertension โ Houston, Texas
- Dual-Language B-MORE for Hypertension โ Orlando, Florida
- Assessing the Feasibility of the "Heart Care Pairs" Intervention โ Birmingham, Alabama
- IMPACT-HTN Study of Patients With Hypertension โ Palo Alto, California
- Genetic Architecture of Natriuretic Peptides and Blood Pressure Response โ Birmingham, Alabama
Explore by condition: All Hypertension (HTN) clinical trials
๐ก How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.