← Back to Search

Behavioral Intervention

Lifestyle Interventions for Chronic Disease

N/A
Waitlist Available
Led By Christopher L Pankey, Ph.D.
Research Sponsored by West Virginia School of Osteopathic Medicine
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be between 18 and 65 years old
Must not have
No chronic disease diagnosis
Unwillingness to participate
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 4 months
Awards & highlights
No Placebo-Only Group

Summary

This trial aims to address chronic diseases in rural areas by increasing physical activity and healthy body composition, as an effective and affordable treatment with fewer side effects than pharmaceuticals.

Who is the study for?
This trial is for rural patients with at least two diagnosed chronic diseases (like obesity, high cholesterol, diabetes) where exercise therapy can help. They need a doctor's referral and must be willing to participate in lifestyle changes.
What is being tested?
The study tests a program that educates these patients on the benefits of physical activity and healthy body composition. It includes advice on local fitness opportunities and training to use exercise equipment comfortably.
What are the potential side effects?
Since this intervention focuses on lifestyle changes rather than medication, side effects are minimal compared to pharmaceuticals. However, individuals may experience typical exercise-related discomfort or injury if not properly guided.

Eligibility Criteria

Exclusion Criteria

You may be eligible for the trial if you check “No” for criteria below:
Select...
I do not have any long-term illnesses.
Select...
I am willing to participate in the trial.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~4 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and 4 months for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Attrition rate
Demand
physical activity
Secondary study objectives
BMI
Blood glucose
Blood pressure
+4 more

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

1Treatment groups
Experimental Treatment
Group I: ActiveExperimental Treatment1 Intervention
participants that have received a referral, and opt-in for the adjunctive treatment plan

Find a Location

Who is running the clinical trial?

West Virginia School of Osteopathic MedicineLead Sponsor
5 Previous Clinical Trials
423 Total Patients Enrolled
Christopher L Pankey, Ph.D.Principal InvestigatorWest Virginia School of Osteopathic Medicine
~45 spots leftby Sep 2025