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Evaluation of the Americans in Motion - Healthy Interventions Project

The Impact of Brief Primary Care Counseling and Novel Physiological Measures on Patient Physical and Emotional Health

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00534482
Acronym
AIM-HI
Enrollment
950
Registered
2007-09-26
Start date
2007-07-31
Completion date
2009-10-31
Last updated
2011-05-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diet, Mental Health, Physical Activity

Keywords

fitness

Brief summary

This research project brings together the American Academy of Family Physicians (AAFP) National Research Network (AAFP-NRN) and the AAFP's public health initiative, Americans In Motion (AIM). This project will develop and evaluate a practice improvement program to improve family physicians' delivery of effective patient-centered behavior change interventions for fitness (physical activity, nutrition and emotional well-being). The investigators seek to develop a unique program that positions fitness in a central role as the treatment of choice when dealing with issues of prevention and treatment of chronic conditions. In addition, this newly developed program is intended to help shift the paradigm of family physicians' use of common advice-giving methods to more effective patient-centered lifestyle counseling. Ultimately, this program will seek to improve care for all patients through fitness-related physician interventions. Outcomes: This study design will allow the investigators to evaluate whether (and how) dissemination of educational materials impacts patient intervention by first engaging clinicians and staff in their personal use of these materials. This project will also evaluate the effects of the behavioral change tools, as well as, the added impact of new physiologic feedback measures (HOMA-IR and NMR Lipoprotein profiles) on physical activity and diet in study participants. Conclusion: Primary care offices can become more effective settings to help patients improve physical activity, diet and emotional well-being. Demonstrating the value and impact of creating healthy offices that endorse and support clinicians, office staff and patients in the use of effective educational materials fits well with the new model of care as part of the AAFP's Future of Family Medicine initiatives, which emphasize the importance of lifestyle decisions and supporting successful changes in behaviors within primary care. This project will help define how to accomplish this.

Detailed description

Study Design: This trial will consist of a two-level randomized controlled trial. The first level of randomization will be performed at the practice level in order to study the impact of involving both clinicians and office staff in making their own personal changes (i.e., creating the healthy office)- a central component of AIM - on the translation of the project's educational tools to patients. The second level of randomization will occur at the patient level comparing two practice level interventions designed to improve nutrition, increase physical activity and improve emotional well-being. Furthermore, the effectiveness of the educational tools will be evaluated on self-reported diet, physical activity and emotional well-being and established physiologic measures on behavioral change. Both arms of the study will receive brief office-based counseling using established tools that have been compiled for this project. Practices will be asked to work on incorporating brief nutrition, physical activity and emotional well-being messages into routine care - either motivational in nature for people not willing to work on lifestyle changes, or goal-oriented for those working on changes. Patients in the intervention arm will also receive feedback concerning changes in two novel physiologic measures that correlate with improved nutrition and increased physical activity.

Interventions

BEHAVIORALEnhanced Office

Clinicians and office staff personally engage in AIM-HI fitness program, and promote program to patients

BEHAVIORALConventional Office

Conventional office: Clinicians and office staff are not personally engaged in the AIM-HI fitness program, but promote program to patients.

BEHAVIORALAIM-HI program with enhanced feedback

Patient receives feedback on two novel indicators of their individual cardiovascular risk that: 1)appear to relate to obesity and lack of physical activity, and 2) may show relatively rapid change with improvements in these areas. These are the Homeostatic Assay - Insulin Resistance or HOMA-IR and Nuclear Molecular Resonance (NMR) lipoprotein profiles (NMRLP). These patients and their physicians also will receive periodic feedback on other outcome measures, including BMI, blood pressure, a 3-minute step test, eating assessment, physical activity assessment, and emotional well-being assessment.

BEHAVIORALAIM-HI program and regular feedback

Patients will not receive feedback on two specific cardiovascular risk indicators (ie, Homeostatic Assay - Insulin Resistance, Nuclear Molecular Resonance lipoprotein profiles). However, patients will receive feedback on Body Mass Index, blood pressure, a 3-minute step test, eating assessment, physical activity assessment, and emotional well-being assessment.

Sponsors

The PepsiCo Foundation
CollaboratorOTHER
American Academy of Family Physicians
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Age 18 or above * BMI greater than or equal to 30 * Able to participate in moderate physical activity including a 3-minute step test without worsening an existing medical condition * Life expectancy of greater than one year * Able to read English or Spanish; and * Able to be contacted via phone for follow-up with project staff

Exclusion criteria

* Too ill to participate * A current diagnosis at the index visit of type 2 diabetes, hyperlipidemia, or coronary heart disease * Doctor's evaluation of patient as not appropriate for physical activity * Not capable of giving informed consent; and * Unable to read English or Spanish, including blindness

Design outcomes

Primary

MeasureTime frame
Aggregate patient assessment of practice involvement in patient health behaviors12 months
Aggregate clinician and practice staff assessment of practice involvement in patient healthy behaviors12 months
Spread of billing codes for physician fitness counseling12 months
Body Mass Indexbaseline, 6, 9, and 12 months
Homeostatic Assay- Insulin Resistancebaseline, 3, 6, 9, and 12 months
Nuclear Molecular Resonance (NMR) Lipoprotein Profilesbaseline, 3, 6, 9, and 12 months
3-Minute Step Testbaseline, 3, 6, 9, and 12 months
Blood Pressurebaseline, 3, 6, 9, and 12 months

Secondary

MeasureTime frame
Perceived competence for maintaining healthy eatingbaseline, 3, 6, 9, and 12 months
Physical activity related itemsbaseline, 3, 6, 9, and 12 months
Functional health statusbaseline, 3, 6, 9, and 12 months
Quality of life and well-beingbaseline, 3, 6, 9, and 12 months
Treatment self-regulation items related to dietbaseline, 3, 6, 9, and 12 months
Treatment self-regulation items related to physical activitybaseline, 3, 6, 9, and 12 months
Perceived competence for maintaining physical activitybaseline, 3, 6, 9, and 12 months
Perceived competence for maintaining emotional healthbaseline, 3, 6, 9, and 12 months
Diet and nutrition related itemsbaseline, 3, 6, 9, and 12 months

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026