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Behavioral Intervention
Online Program for Chronic Disease Risk Reduction
N/A
Waitlist Available
Research Sponsored by Florida State University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline, post-intervention (six weeks from baseline) and 4 weeks post-intervention (10 weeks from baseline).
Awards & highlights
Study Summary
This trial tests if an online program can help rural adults reduce their risk of chronic diseases.
Who is the study for?
This trial is for adults over 18 living in rural southern areas (RUCC 4-9) with internet access and at least one chronic disease risk factor or diagnosis. It's not open to those under 18 or non-rural residents.Check my eligibility
What is being tested?
The study is examining a web-based intervention designed to reduce the risk of chronic diseases among rural adults, using online tools accessible via computer or smartphone.See study design
What are the potential side effects?
Since this trial involves a web-based educational program rather than medication, traditional side effects are not applicable. However, participants may experience screen fatigue or stress from lifestyle changes.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline, post-intervention (six weeks from baseline) and 4 weeks post-intervention (10 weeks from baseline).
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline, post-intervention (six weeks from baseline) and 4 weeks post-intervention (10 weeks from baseline).
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Change in Dietary Fat Intake from Baseline to Post-intervention and 4 weeks post-intervention
Change in Exercise from Baseline to Post-intervention and 4 weeks post-intervention
Change in Health Habits and Knowledge from Baseline to Post-intervention and 4 weeks post-intervention
+2 moreSecondary outcome measures
Change in Sleep from Baseline to Post-intervention and 4 weeks post-intervention
Change in Social Support from Baseline to Post-intervention and 4 weeks post-intervention
Change in Social Support to Eat Better and Move More from Baseline to Post-intervention and 4 weeks post-intervention
+2 moreTrial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: InterventionExperimental Treatment1 Intervention
The participants in the intervention group received the chronic disease risk reduction intervention.
Group II: ControlActive Control1 Intervention
The participant in the control group receive usual care.
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Who is running the clinical trial?
Florida State UniversityLead Sponsor
203 Previous Clinical Trials
31,716 Total Patients Enrolled
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Eligibility Criteria:
This trial includes the following eligibility criteria:- I am under 18 years old.I am 18 years old or older.
Research Study Groups:
This trial has the following groups:- Group 1: Control
- Group 2: Intervention
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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