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Recruiting NCT07114822

HOPE Intervention for Fitness

No phase Interventional Diabetes Mellitus Type 2

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Harnessing Online Peer Education.
Who it may be relevant to
Registry conditions: Diabetes Mellitus Type 2. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Harnessing Online Peer Education For Fitness in People With Type II Diabetes

Overview

We will test the HOPE intervention on changing behavior of people to exercise more (take more steps each day).

Interventions

  • Behavioral Harnessing Online Peer Education
    This group will have peer leaders that will engage participants in the groups. These peer leaders are those with type II diabetes that have over the recommended amount of exercise each week.

Primary outcome measures

  • Step Count [Time frame: 1 month]
Secondary outcome measures (3)
  • Average fasting glucose [Time frame: 1 week]
  • HbA1c [Time frame: Baseline]
  • Change in weight and Body Mass Index (BMI) [Time frame: 1 month]

Eligibility criteria

Inclusion criteria

  • 18 years or older
  • Living in the US
  • Self-report diagnosis of type II diabetes
  • Has an app to track step count

Exclusion criteria

  • On insulin or an injectable weight loss drug

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Prevention

Study locations

United States · 1 center
  • UC Irvine — Irvine

Identifiers

NCT: NCT07114822 · 7008

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗