PA Moves Trial - PCP Participants

NCT ID: NCT05319821

Last Updated: 2026-01-08

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

ACTIVE_NOT_RECRUITING

Clinical Phase

NA

Total Enrollment

48 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-09-21

Study Completion Date

2028-02-29

Brief Summary

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The purpose of this voluntary research study is to determine the impact of an ECHO intervention on the likelihood that rural primary care providers (PCP) will refer their physically inactive patients to be more active.

Detailed Description

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People living in rural areas are diagnosed and die from cancer at higher rates than people living in cities. Physical activity has been shown to decrease the risk and occurrence of a variety of cancers, including bladder, breast, colon, endometrial, gastric, kidney, and prostate cancers. Being inactive can cause over 10% of breast and colon cancer cases.

Compared to people living in cities, people living in rural areas tend to be less physically active. They're also more likely to be overweight/obese or have diabetes. Adults who are overweight, obese, or diabetic often have changes in the way their bodies deal with insulin, glucose metabolism, and inflammation. Physical activity is thought to reduce the risk of cancer by improving these issues over time.

PCPs and their staff can identify a patient's need for more physical activity, but may not have the time or resources to give advice or assistance. We have set up a telephone-based physical activity coaching program, called the MoveLine, to give inactive patients advice and assistance in becoming more physically active.

The purpose of this study is to determine if an ECHO intervention will impact the likelihood that PCPs will refer patients to the MoveLine for physical activity coaching.

Approximately 32-48 providers will take part in this research study.

Conditions

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Behavior Physical Activity

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

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Active Intervention

PCP participants in the practice cohort or the intervention group will receive the ECHO46 intervention via real-time, interactive videoconferencing through Zoom sessions held once weekly for 4 weeks (4 sessions total) at regularly scheduled times convenient to providers. Session topics will focus on training PCP participants to assess, advise, and refer patients to be more physically active, as well as provide evidence-based strategies they can use to supplement and sustain their communication efforts.

Group Type ACTIVE_COMPARATOR

Receive ECHO training

Intervention Type BEHAVIORAL

Active Intervention

Delayed Intervention

PCP participants will be offered the intervention in year 5.

Group Type ACTIVE_COMPARATOR

Offered ECHO training in year 5

Intervention Type BEHAVIORAL

Delayed Intervention

Interventions

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Receive ECHO training

Active Intervention

Intervention Type BEHAVIORAL

Offered ECHO training in year 5

Delayed Intervention

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

1. Primary care providers or adjunct faculty from Primary Health Network (PHN) or UPMC clinics serving rural populations
2. Must be able to provide and understand informed consent

Exclusion Criteria

1\. Primary care providers or adjunct faculty NOT from PHN or UPMC clinics
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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National Cancer Institute (NCI)

NIH

Sponsor Role collaborator

University of Pittsburgh

OTHER

Sponsor Role lead

Responsible Party

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Kathryn Schmitz

Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Kathryn Schmitz, PhD

Role: PRINCIPAL_INVESTIGATOR

University of Pittsburgh

Locations

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Milton S. Hershey Medical Center

Hershey, Pennsylvania, United States

Site Status

UPMC

Pittsburgh, Pennsylvania, United States

Site Status

Countries

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United States

Other Identifiers

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R01CA268017

Identifier Type: NIH

Identifier Source: secondary_id

View Link

STUDY22110036

Identifier Type: -

Identifier Source: org_study_id

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