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Multimedia Lifestyle Improvement for Cardiovascular Disease (SAHARA Trial)

N/A
Waitlist Available
Led By Sonia Anand, MD, PhD
Research Sponsored by McMaster University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Greater than or equal to 30 years of age
No previous cardiovascular disease
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline and 12 months from randomization
Awards & highlights

SAHARA Trial Summary

This trial is testing whether a multimedia health behavior intervention can reduce cardiac risk factors in South Asians, who are a group that is especially at risk for developing these factors at younger ages and at lower body weights.

Who is the study for?
The SAHARA-Trial is for South Asian individuals aged 30 or older living in Ontario or British Columbia, who have not had cardiovascular disease and are not currently pregnant. Participants must be able to use the internet, email, and multimedia devices.Check my eligibility
What is being tested?
This trial tests a 12-month interactive multimedia program designed to improve smoking habits, diet, and physical activity against usual care. It also examines if knowing one's genetic risk for heart attack affects behavior change and cardiac risk factors.See study design
What are the potential side effects?
Since this trial involves lifestyle improvements through an educational intervention rather than medication, side effects are minimal but may include the stress of lifestyle changes or discomfort from increased physical activity.

SAHARA Trial Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
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I am 30 years old or older.
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I have never had heart disease.

SAHARA Trial Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline and 12 months from randomization
This trial's timeline: 3 weeks for screening, Varies for treatment, and baseline and 12 months from randomization for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Effectiveness of a 12 Month Culturally-Specific Multi-media Intervention on Heart Health Risk
Secondary outcome measures
Change in Diabetes Status
Change in Hypertension Status
Myocardial Infarction

SAHARA Trial Design

2Treatment groups
Active Control
Placebo Group
Group I: Multimedia Lifestyle ImprovementActive Control1 Intervention
Includes goal setting, self monitoring and participants will receive regular health messaging using electronic media regarding smoking, dietary habits & physical activity
Group II: Usual CarePlacebo Group1 Intervention
Includes usual advice and no regular health messaging.

Find a Location

Who is running the clinical trial?

McMaster UniversityLead Sponsor
880 Previous Clinical Trials
2,597,485 Total Patients Enrolled
Sonia Anand, MD, PhDPrincipal InvestigatorMcMaster University; Hamilton Health Sciences; Population Health Research Institute
1 Previous Clinical Trials
400 Total Patients Enrolled

Media Library

Multimedia Lifestyle Improvement Clinical Trial Eligibility Overview. Trial Name: NCT01841398 — N/A
Cardiovascular Disease Research Study Groups: Multimedia Lifestyle Improvement, Usual Care
Cardiovascular Disease Clinical Trial 2023: Multimedia Lifestyle Improvement Highlights & Side Effects. Trial Name: NCT01841398 — N/A
Multimedia Lifestyle Improvement 2023 Treatment Timeline for Medical Study. Trial Name: NCT01841398 — N/A

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Are there still vacancies for individuals to participate in this trial?

"An examination of clinicaltrials.gov reveals that the study is no longer accepting participants, as it was last modified on June 8th 2016. Despite this, 600 other studies are still currently seeking enrolment from patients."

Answered by AI

What criteria must participants meet to join this research program?

"This study is seeking 343 participants between the ages of 30 and 70 who suffer from both obesity and visceral fat. To be accepted, candidates must meet these requirements."

Answered by AI

Is the cohort for this trial inclusive of geriatric patients?

"In accordance with the conditions for inclusion, prospective participants must be between 30 and 70 years old."

Answered by AI
~27 spots leftby Apr 2025