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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 weeks
Treatment ~ Varies
Follow Up ~baseline, post-intervention (six weeks from baseline) and 4 weeks post-intervention (10 weeks from baseline).
This trial's timeline: 3 weeks for screening, Varies for treatment, and baseline, post-intervention (six weeks from baseline) and 4 weeks post-intervention (10 weeks from baseline). for reporting.

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 more
Secondary 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 more

Trial 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.

Find a Location

Who is running the clinical trial?

Florida State UniversityLead Sponsor
198 Previous Clinical Trials
30,606 Total Patients Enrolled

Media Library

Chronic Disease Risk Reduction (Behavioral Intervention) Clinical Trial Eligibility Overview. Trial Name: NCT05611580 — N/A
Chronic Disease Research Study Groups: Control, Intervention
Chronic Disease Clinical Trial 2023: Chronic Disease Risk Reduction Highlights & Side Effects. Trial Name: NCT05611580 — N/A
Chronic Disease Risk Reduction (Behavioral Intervention) 2023 Treatment Timeline for Medical Study. Trial Name: NCT05611580 — N/A

Frequently Asked Questions

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

What is the cap on recruitment for this research trial?

"Affirmative, according to records hosted on clinicaltrials.gov this research endeavour is presently recruiting patients who meet the eligibility criteria. The trial was originally posted on January 1st 2023 and recently updated November 3rd 2022; it requires 80 volunteers from a single site."

Answered by AI

Are enrollments currently open for this clinical research?

"Affirmative, according to data hosted on clinicaltrials.gov this research has been actively recruiting since its inception on January 1st 2023 and is currently looking for 80 participants from a single site."

Answered by AI

What are the primary investigations that this trial is attempting to elucidate?

"This trial aims to evaluate the change in health habits and knowledge from baseline to post-intervention, as well as 4 weeks past intervention. Secondary outcomes include changes in social support to eat better and move more (in terms of informational, emotional, and encouragement) from baseline to post-intervention and 4 weeks after; interpersonal support evaluation list scores; perceived belonging, tangible, appraisal supports over time; along with levels of stress pre & post treatment."

Answered by AI
~5 spots leftby May 2024