Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06028503

ACT Intervention for Type 2 Diabetes Management for Rural and Underserved Community

Led by Sam Houston State University · Updated on 2025-05-15

60

Participants Needed

1

Research Sites

178 weeks

Total Duration

On this page

Sponsors

S

Sam Houston State University

Lead Sponsor

C

Chelsea Ratcliff, Ph.D.

Collaborating Sponsor

AI-Summary

What this Trial Is About

The purpose of this project is to examine the feasibility/acceptability of a one-day Acceptance and Commitment Therapy + Lifestyle Education group intervention paired with 12-weeks of Continuous Glucose Monitoring for patients with type 2 diabetes (T2D) living in rural communities. This study is being designed as a randomized control trial (RCT) comparing ACT+LE+CGM to LE+CGM to LE. The ultimate goal of this line of research is that a community-wide intervention of Acceptance and Commitment Therapy (ACT) with Continuous Glucose Monitoring (CGM) and Lifestyle Education (LE) will improve T2D outcomes in rural communities compared to CGM and LE, or LE alone. Our goal is to develop a scalable and sustainable program for diabetes management in rural areas that enables individual self-management and does not require extensive healthcare resources in an existing medical desert.

CONDITIONS

Official Title

ACT Intervention for Type 2 Diabetes Management for Rural and Underserved Community

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosed diabetes (self-reported) with an HbA1c of 6.0 or higher using a point-of-care device
  • At least 18 years of age or older
  • Able to speak English
  • Able to provide informed consent and participate in the study
  • Reliable access to a personal smartphone device
  • Residence zip code associated with a rural area
Not Eligible

You will not qualify if you...

  • Reported suicidal ideation at the initial visit
  • Evidence of acute psychosis preventing informed consent
  • Cognitive impairment preventing informed consent
  • Heavy use of alcohol or other substances
  • Medically too complex for conservative treatment as determined by the study team
  • Presence of a pacemaker or other implanted electrical medical device
  • Pregnancy
  • Under 18 years old
  • Non-English speaking individuals (protocol not validated in other languages)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Trial Site Locations

Total: 1 location

1

Sam Houston State University College of Osteopathic Medicine

Conroe, Texas, United States, 77304

Actively Recruiting

Loading map...

Research Team

R

Ryan J Marek, Ph.D.

CONTACT

C

Chelsea Ratcliff, Ph.D.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

FACTORIAL

Primary Purpose

TREATMENT

Number of Arms

3

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here