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The Impact of Integrating an Internet Weight Control Program Into Primary Care

Primary Purpose

Overweight, Obese

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Usual Care
Brief Physician Counseling
Referral and access to an internet weight control program
Brief follow up email notes from PCPs
Sponsored by
Milton S. Hershey Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Overweight

Eligibility Criteria

21 Years - 70 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

INCLUSION CRITERIA:

Physicians and Mid-level providers (Focus group and RCT):

  • Has medical license to practice primary care
  • Practice within 60 miles (focus group)/100 miles (RCT) of Penn State Hershey Medical Center
  • Practice not located at Penn State Hershey Medical Center campus (focus group)
  • Be active primary care providers (provide primary care at least 2 half days per week at one practice)
  • Not have had completed a weight management fellowship
  • Use internet in their office

Patients (Focus group only):

  • Ages 21-60
  • Body Mass Index between 25.0-50.0 kg/m2
  • Have internet access at home or work
  • Patient of a primary care provider who practices Internal Medicine or Family Community Medicine
  • Has seen primary care provider in the last year, not including acute care

Patients (RCT only)

  • Ages 21-70
  • Body Mass Index between 25.0-50.0 kg/m2
  • Have internet access at home or work
  • Patient of a PCP who is participating in the study
  • Patient has been seeing the PCP for at least 12 months and has no other PCP
  • The PCP must approve the patients' participation

EXCLUSION CRITERIA:

Physicians and Mid-level providers (RCT only)

  • Practice serves a specialty care population
  • Pregnant or planning to become pregnant in the next 3 months
  • Planning on changing practice locations in the next 12 months
  • Planning on retiring in the next 12 months

Patients (Focus group and RCT)

  • Losing >5% of current body weight in the previous 6 months
  • Participating in a research project involving weight loss or physical activity in the previous 6 months
  • Pregnancy during the previous 6 months, lactating, or planning to become pregnant in the next 3 months (focus group)/12 months (RCT)
  • Planning on moving out of the area in the next 3 months (focus group)/12 months (RCT)
  • Current treatment for a condition or with a medication that could impact weight (Orlistat - aka. Alli, Phentermine, Topiramate - aka. Topamax) and are not willing to stop for duration of the study
  • Hospitalization for psychiatric problems during the prior year

Patients (RCT only)

  • Had weight loss surgery
  • Planning on changing primary care provider in the next 12 months
  • Participating in an online or community weight loss program (e.g., Weight Watchers) and not willing to stop for the duration of the study
  • Doctor has diagnosed a heart condition and said should only do physical activity recommended by doctor
  • Feel pain in chest when doing physical activity
  • In the past month, have had chest pain when not doing physical activity
  • In the end stages of renal, liver or kidney diseases
  • Has heart failure
  • Has/had cancer in past 5 years (except non-melanoma skin cancer)
  • Cannot walk for exercise for 10 minutes
  • Not willing to participate in 12-month intervention
  • Taking insulin
  • Treated for or diagnosed with an eating disorder
  • Diagnosed with HIV
  • Two weeks of steroid use in past year

Sites / Locations

  • Penn State Hershey Medical Center

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Experimental

Experimental

Arm Label

Brief physician counseling (BPC) + Usual care (UC)

BPC + Internet Weight Control Program (IWCP)

BPC + IWCP + Follow up email notes from PCP

Arm Description

The participant will receive standard care. They will receive BPC from their PCP on weight loss by reviewing a goal setting worksheet and collaboratively setting a goal for weight loss.

The participant will receive BPC from their PCP by reviewing a goal setting worksheet and collaboratively setting a goal for weight loss. They will receive referral and access to an internet weight control program.

The participant will receive BPC form their PCP by reviewing a goal setting worksheet and collaboratively setting a goal for weight loss. They will receive referral and access to an internet weight control program. And they will receive brief follow up email notes from PCPs on how their weight loss is going (from data collected from the weight loss website).

Outcomes

Primary Outcome Measures

Body Weight
Body weight and height will be measured by a research assistant using a portable, calibrated stadiometer (Tanita, Inc). Waist circumference will be measured using standard procedures, recorded to the nearest millimeter.

Secondary Outcome Measures

Block Food Frequency Questionnaire
This questionnaire asks participants to estimate how often they consume a variety of specific foods.
Paffenbarger Activity Questionnaire
This instrument has been used to estimate leisure time activity in many studies of weight loss (78, 112-113) and changes in energy expenditure using this measure correlate with changes in body weight over at least an 18 month period (114). A scoring algorithm allows the calculation of caloric expenditure overall as well as in activities of light, medium and high intensity.
Patterns of medical care
After 12 months, data will be collected from medical charts using a standardized form to identify: 1) number of PCP visits, 2) use of any approved (e.g., Xenical) or off-label (e.g., Topiramate) weight loss medications after randomization, and 3) evaluations by a surgical weight control program.
Use of the 5 A's during PCP Visits
After the index PCP visit and quarterly, subjects will complete a survey detailing the use the 5 A's (Ask, Advise, Assess, Assist and Arrange) during visits. Within 24-72 hours after the index visit, subjects will be called to complete the exit interview.
Sociodemographics and tobacco use
Age, gender, race and ethnicity, smoking status, education and other demographics, will be measured based on standard self-report.
Weight History Questionnaire
To measure past weight, past weight loss attempts and methods used to lose weight in the past, we will use the Weight History Questionnaire (WHQ) from the National Health and Nutrition Examination Survey (NHANES).
Health Literacy
To measure health literacy, the Newest Vital Sign (NVS), a nutrition label that is accompanied by 6 questions that requires 3 minutes for administration will be used.
Three-Factor Eating Questionnaire (TFEQ)
The TFEQ measures three dimensions of dietary restraint: cognitive restraint, disinhibition, perceived hunger.
Depressive Symptoms
Depressive symptoms have been associated with body weight changes, so these symptoms will be measured with the 20-item Centers for Epidemiological Studies Depression Scale (CES-D). *If a patient scores a 25 or higher on the scale, research staff will notify their primary care physician; however, this does not make them ineligible for the study.
Treatment Self-Regulation Scale (TSRQ)
The TSRQ will be used to measure autonomous (5 items) versus controlled (8 items) motivations, as well as total motivation (autonomous + controlled).
Weight Control Self-Efficacy
Perceived competence in weight control will be measured using the Efficacy Life-Style Questionnaire (WEL). The WEL is a 20-item instrument consisting of five situational factors (Negative Emotions, Availability, Social Pressure, Physical Discomfort, and Positive Activities).
Patient Satisfaction and Accountability
Patient satisfaction will be measured with the Patient Satisfaction Questionnaire 18 (PSQ18), which includes scales to measure technical quality, interpersonal manner, communication and time spent with the doctor with scale reliability between 0.79 and 0.93. Accountability will be measured with a 6-item measure developed by Mohr and colleagues (consultant), which measures the extent to which subjects believe that they are being monitored and the extent to which they are concerned about being judged by the monitor.
Sedentary Behavior
This validated questionnaire asks participants about the duration of specific sedentary behaviors during a typical weekday and weekend day.
Physical Activity Self Efficacy
This questionnaire asks about participants about their level of confidence in doing physical activity in certain situations.
Eating Behavior Inventory
The Eating Behavior Inventory (EBI) is a validated questionnaire used by obesity researchers to measure the adoption of specific behaviors linked with weight-loss success.
Internet Usage
This questionnaire asks participants about the frequency of their Internet use and the ways in which they use the Internet
Analysis of text edits in PCP emails
We will analyze 100% of the personal notes added by PCPs to messages sent to patients in Condition C. Using a grounded theory approach, Dr. Hwang will analyze the content in the notes from PCPs and create a codebook and categories for these notes.
Blood pressure
Blood pressure will be measured by a research assistant using an automatic blood pressure monitor (Omron) and standard procedures.
Adherence (logins to website)
We will examine login data (overall and percentage of weeks logging in) as a mean and median, as well as a monthly percentage.
Medication
Participants will be asked to bring their current prescription medications. The research coordinator will record the name and dose of each.

Full Information

First Posted
May 24, 2012
Last Updated
December 6, 2016
Sponsor
Milton S. Hershey Medical Center
Collaborators
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), University of North Carolina, Chapel Hill, The University of Texas Health Science Center, Houston
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1. Study Identification

Unique Protocol Identification Number
NCT01606813
Brief Title
The Impact of Integrating an Internet Weight Control Program Into Primary Care
Official Title
The Impact of Integrating an Internet Weight Control Program Into Primary Care
Study Type
Interventional

2. Study Status

Record Verification Date
December 2016
Overall Recruitment Status
Completed
Study Start Date
October 2012 (undefined)
Primary Completion Date
November 2016 (Actual)
Study Completion Date
November 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Milton S. Hershey Medical Center
Collaborators
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), University of North Carolina, Chapel Hill, The University of Texas Health Science Center, Houston

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The investigators will conduct a randomized controlled trial comparing the effects of three interventions on weight loss at 12 months. The investigators propose to test the impact of integrating an effective automated Internet weight control program into primary care by recruiting patients and randomizing them to one of three conditions: A) Brief physician counseling plus usual care, B) Brief physician counseling plus referral and access to the Internet weight control program and, C) Brief physician counseling plus referral and access to the Internet weight control program plus brief follow-up email notes of support and accountability from Primary Care Physicians. The investigators hypothesize that an online program for weight control can be more effective by enhancing online follow-up with PCPs.
Detailed Description
Every year, roughly 700 of the 750 million visits that overweight and obese patients make with primary care providers (PCPs) occur without any weight counseling. The main reasons for this are that PCPs are poorly trained to help their patients lose weight and that there are no consistently effective interventions for primary care settings. Though in-person and telephone-based weight control programs have been difficult to disseminate in primary care, online weight control programs are increasingly effective and may lend themselves to be used in these settings. Given the growing number of effective online programs, for obesity and for other conditions seen in primary care (e.g., depression, insomnia) it is important to understand whether these programs can be effective when integrated into primary care and whether they are enhanced by provider involvement. Research on the 5 A's model of primary care behavior change suggests that the most effective, yet least used feature of primary care interventions is arranging follow-up, where providers hold patients accountable to adhering to treatments and achieving specific outcomes. The 5 A's model provides a useful framework for integrating behavior change interventions into primary care. In this model, providers ASK about weight, ADVISE patients to lose weight, ASSESS readiness to change, ASSIST the patient in making changes and ARRANGE follow-up. Unfortunately, though PCPs are uniquely positioned to ARRANGE follow-up, given their long-term relationship with the patient, and studies show that ARRANGING follow-up may be the most effective of the 5 A's, it is the least often used. In a study of 481 encounters with overweight patients, Pollak (Consultant) and colleagues observed that PCPs ARRANGED follow-up in only 5% of visits, though it was the only one of the 5 A's associated with future weight loss. Kottke and colleagues similarly observed that primary care smoking cessation interventions that included more "reinforcing sessions" with PCPs were the most effective. This is consistent with conclusions by Whitlock and colleagues that "Simply notifying patients that follow-up will occur seems to be a powerful motivating factor". These findings have been extended to online interventions, where two meta-analyses concluded that the impact of online interventions for depression and anxiety is enhanced by follow-up that includes being accountable to and supported by a human being. The investigators have created a simple method for integrating an Internet weight control program into primary care settings, by allowing PCPs to monitor their patients' adherence and outcomes and email them pre-written, tailored follow-up messages. PCPs in the investigators' pilot work believed that this would help to overcome key barriers to helping their patients lose weight.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Overweight, Obese

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Factorial Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
611 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Brief physician counseling (BPC) + Usual care (UC)
Arm Type
Active Comparator
Arm Description
The participant will receive standard care. They will receive BPC from their PCP on weight loss by reviewing a goal setting worksheet and collaboratively setting a goal for weight loss.
Arm Title
BPC + Internet Weight Control Program (IWCP)
Arm Type
Experimental
Arm Description
The participant will receive BPC from their PCP by reviewing a goal setting worksheet and collaboratively setting a goal for weight loss. They will receive referral and access to an internet weight control program.
Arm Title
BPC + IWCP + Follow up email notes from PCP
Arm Type
Experimental
Arm Description
The participant will receive BPC form their PCP by reviewing a goal setting worksheet and collaboratively setting a goal for weight loss. They will receive referral and access to an internet weight control program. And they will receive brief follow up email notes from PCPs on how their weight loss is going (from data collected from the weight loss website).
Intervention Type
Other
Intervention Name(s)
Usual Care
Intervention Description
Standard care
Intervention Type
Behavioral
Intervention Name(s)
Brief Physician Counseling
Intervention Description
Primary Care Physician (PCP) will review a goal setting worksheet for weight loss with the participant and then collaboratively set a goal for weight loss.
Intervention Type
Behavioral
Intervention Name(s)
Referral and access to an internet weight control program
Intervention Description
Participants will receive a login and password for the weight loss website. The website will encourage patients to set a new weight goal every 3 months and work towards a total weight loss goal of 10%. Patients will also receive an email prompt each week alerting them to new content and reminding them to check-in to the website to report their weight, intake and activity.
Intervention Type
Behavioral
Intervention Name(s)
Brief follow up email notes from PCPs
Intervention Description
Patients will receive a biweekly email from their primary care physician on how they are doing with their weight loss.
Primary Outcome Measure Information:
Title
Body Weight
Description
Body weight and height will be measured by a research assistant using a portable, calibrated stadiometer (Tanita, Inc). Waist circumference will be measured using standard procedures, recorded to the nearest millimeter.
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Block Food Frequency Questionnaire
Description
This questionnaire asks participants to estimate how often they consume a variety of specific foods.
Time Frame
12 months
Title
Paffenbarger Activity Questionnaire
Description
This instrument has been used to estimate leisure time activity in many studies of weight loss (78, 112-113) and changes in energy expenditure using this measure correlate with changes in body weight over at least an 18 month period (114). A scoring algorithm allows the calculation of caloric expenditure overall as well as in activities of light, medium and high intensity.
Time Frame
12 months
Title
Patterns of medical care
Description
After 12 months, data will be collected from medical charts using a standardized form to identify: 1) number of PCP visits, 2) use of any approved (e.g., Xenical) or off-label (e.g., Topiramate) weight loss medications after randomization, and 3) evaluations by a surgical weight control program.
Time Frame
6 months
Title
Use of the 5 A's during PCP Visits
Description
After the index PCP visit and quarterly, subjects will complete a survey detailing the use the 5 A's (Ask, Advise, Assess, Assist and Arrange) during visits. Within 24-72 hours after the index visit, subjects will be called to complete the exit interview.
Time Frame
12 months
Title
Sociodemographics and tobacco use
Description
Age, gender, race and ethnicity, smoking status, education and other demographics, will be measured based on standard self-report.
Time Frame
12 months
Title
Weight History Questionnaire
Description
To measure past weight, past weight loss attempts and methods used to lose weight in the past, we will use the Weight History Questionnaire (WHQ) from the National Health and Nutrition Examination Survey (NHANES).
Time Frame
12 months
Title
Health Literacy
Description
To measure health literacy, the Newest Vital Sign (NVS), a nutrition label that is accompanied by 6 questions that requires 3 minutes for administration will be used.
Time Frame
12 months
Title
Three-Factor Eating Questionnaire (TFEQ)
Description
The TFEQ measures three dimensions of dietary restraint: cognitive restraint, disinhibition, perceived hunger.
Time Frame
12 months
Title
Depressive Symptoms
Description
Depressive symptoms have been associated with body weight changes, so these symptoms will be measured with the 20-item Centers for Epidemiological Studies Depression Scale (CES-D). *If a patient scores a 25 or higher on the scale, research staff will notify their primary care physician; however, this does not make them ineligible for the study.
Time Frame
12 months
Title
Treatment Self-Regulation Scale (TSRQ)
Description
The TSRQ will be used to measure autonomous (5 items) versus controlled (8 items) motivations, as well as total motivation (autonomous + controlled).
Time Frame
12 months
Title
Weight Control Self-Efficacy
Description
Perceived competence in weight control will be measured using the Efficacy Life-Style Questionnaire (WEL). The WEL is a 20-item instrument consisting of five situational factors (Negative Emotions, Availability, Social Pressure, Physical Discomfort, and Positive Activities).
Time Frame
12 months
Title
Patient Satisfaction and Accountability
Description
Patient satisfaction will be measured with the Patient Satisfaction Questionnaire 18 (PSQ18), which includes scales to measure technical quality, interpersonal manner, communication and time spent with the doctor with scale reliability between 0.79 and 0.93. Accountability will be measured with a 6-item measure developed by Mohr and colleagues (consultant), which measures the extent to which subjects believe that they are being monitored and the extent to which they are concerned about being judged by the monitor.
Time Frame
12 months
Title
Sedentary Behavior
Description
This validated questionnaire asks participants about the duration of specific sedentary behaviors during a typical weekday and weekend day.
Time Frame
12 months
Title
Physical Activity Self Efficacy
Description
This questionnaire asks about participants about their level of confidence in doing physical activity in certain situations.
Time Frame
12 months
Title
Eating Behavior Inventory
Description
The Eating Behavior Inventory (EBI) is a validated questionnaire used by obesity researchers to measure the adoption of specific behaviors linked with weight-loss success.
Time Frame
12 months
Title
Internet Usage
Description
This questionnaire asks participants about the frequency of their Internet use and the ways in which they use the Internet
Time Frame
12 months
Title
Analysis of text edits in PCP emails
Description
We will analyze 100% of the personal notes added by PCPs to messages sent to patients in Condition C. Using a grounded theory approach, Dr. Hwang will analyze the content in the notes from PCPs and create a codebook and categories for these notes.
Time Frame
12 months
Title
Blood pressure
Description
Blood pressure will be measured by a research assistant using an automatic blood pressure monitor (Omron) and standard procedures.
Time Frame
12 months
Title
Adherence (logins to website)
Description
We will examine login data (overall and percentage of weeks logging in) as a mean and median, as well as a monthly percentage.
Time Frame
12 months
Title
Medication
Description
Participants will be asked to bring their current prescription medications. The research coordinator will record the name and dose of each.
Time Frame
12 Months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
INCLUSION CRITERIA: Physicians and Mid-level providers (Focus group and RCT): Has medical license to practice primary care Practice within 60 miles (focus group)/100 miles (RCT) of Penn State Hershey Medical Center Practice not located at Penn State Hershey Medical Center campus (focus group) Be active primary care providers (provide primary care at least 2 half days per week at one practice) Not have had completed a weight management fellowship Use internet in their office Patients (Focus group only): Ages 21-60 Body Mass Index between 25.0-50.0 kg/m2 Have internet access at home or work Patient of a primary care provider who practices Internal Medicine or Family Community Medicine Has seen primary care provider in the last year, not including acute care Patients (RCT only) Ages 21-70 Body Mass Index between 25.0-50.0 kg/m2 Have internet access at home or work Patient of a PCP who is participating in the study Patient has been seeing the PCP for at least 12 months and has no other PCP The PCP must approve the patients' participation EXCLUSION CRITERIA: Physicians and Mid-level providers (RCT only) Practice serves a specialty care population Pregnant or planning to become pregnant in the next 3 months Planning on changing practice locations in the next 12 months Planning on retiring in the next 12 months Patients (Focus group and RCT) Losing >5% of current body weight in the previous 6 months Participating in a research project involving weight loss or physical activity in the previous 6 months Pregnancy during the previous 6 months, lactating, or planning to become pregnant in the next 3 months (focus group)/12 months (RCT) Planning on moving out of the area in the next 3 months (focus group)/12 months (RCT) Current treatment for a condition or with a medication that could impact weight (Orlistat - aka. Alli, Phentermine, Topiramate - aka. Topamax) and are not willing to stop for duration of the study Hospitalization for psychiatric problems during the prior year Patients (RCT only) Had weight loss surgery Planning on changing primary care provider in the next 12 months Participating in an online or community weight loss program (e.g., Weight Watchers) and not willing to stop for the duration of the study Doctor has diagnosed a heart condition and said should only do physical activity recommended by doctor Feel pain in chest when doing physical activity In the past month, have had chest pain when not doing physical activity In the end stages of renal, liver or kidney diseases Has heart failure Has/had cancer in past 5 years (except non-melanoma skin cancer) Cannot walk for exercise for 10 minutes Not willing to participate in 12-month intervention Taking insulin Treated for or diagnosed with an eating disorder Diagnosed with HIV Two weeks of steroid use in past year
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Christopher Sciamanna, MD, MPH
Organizational Affiliation
Milton S. Hershey Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Penn State Hershey Medical Center
City
Hershey
State/Province
Pennsylvania
ZIP/Postal Code
17033
Country
United States

12. IPD Sharing Statement

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The Impact of Integrating an Internet Weight Control Program Into Primary Care

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