search
Back to results

Communication & Peer Support Effects on Physical Activity in Overweight Postmenopausal Women (BePHIT)

Primary Purpose

Healthy, Obesity, Postmenopausal

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
communication intervention
exercise intervention
Sponsored by
Ohio State University Comprehensive Cancer Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Healthy focused on measuring Feasibility study, Interactive voice response system (IVR), health coach, no evidence of disease

Eligibility Criteria

55 Years - 75 Years (Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Present a letter/documentation from a primary physician stating that they can participate in a physical activity program that will require walking up to 10,000 steps per day
  • Have a body mass index (BMI) between 25 and 40 kg/m^2 (inclusive)
  • Be postmenopausal, defined as no period for 12 months if over age 55, or no period for 12 months; also, women who have had their ovaries removed will be considered as postmenopausal
  • Willing to participate in a wellness program that lasts 12 weeks and involves walking for at least 30 minutes a day on most days
  • Has access to a cell phone during the 12-week intervention
  • Functional knowledge of English (ability to both read and write)

Exclusion Criteria:

  • Taking hormone replacement therapy within 3 months of enrollment
  • Taking Tamoxifen or Raloxifene within 3 months of enrollment
  • Enrolled in a weight management program, such as Weight Watchers
  • Engaged in regular, planned walking of at least 30 minutes a day
  • Previous history of breast cancer
  • Premenopausal
  • Age > 75 years, to minimize co-morbidities
  • Cannot walk one mile

Sites / Locations

  • Ohio State University Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Arm I (health coach)

Arm II (no coach condition)

Arm Description

Participants participate in a 12-week physical activity intervention (walking program)and receive health mail messages via IVR system and from a health coach. Participants in this arm of the study, interacted with the IVR system and had the option of interacting with the health coach.

Participants participate in a 12-week physical activity intervention (walking program)and receive health mail messages via IVR system. Participants in this arm of the study only interacted with the IVR system.

Outcomes

Primary Outcome Measures

Change in time taken to complete a one mile walk.

Secondary Outcome Measures

Changes in anthropometrics, psychometrics and the benefits of a health coach.
Weekly effectiveness (satisfaction, convenience, ease of operation) of all the materials and processes as assessed by questionnaires.
If the self-reported steps per day, derived from daily activity logs, relates to the change in performance on the 1-mile walk test between baseline and end of study.
The steps walked per day and the change in performance on the 1-male walk test are both outcomes.

Full Information

First Posted
July 13, 2013
Last Updated
June 26, 2020
Sponsor
Ohio State University Comprehensive Cancer Center
Collaborators
Breast Cancer Research Foundation
search

1. Study Identification

Unique Protocol Identification Number
NCT01940016
Brief Title
Communication & Peer Support Effects on Physical Activity in Overweight Postmenopausal Women
Acronym
BePHIT
Official Title
A Feasibility Study on the Effects of Tailored Communication and Health Coach Support on Physical Activity in Overweight Postmenopausal Women: BePHIT
Study Type
Interventional

2. Study Status

Record Verification Date
June 2020
Overall Recruitment Status
Completed
Study Start Date
April 1, 2007 (Actual)
Primary Completion Date
November 1, 2009 (Actual)
Study Completion Date
November 1, 2009 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Ohio State University Comprehensive Cancer Center
Collaborators
Breast Cancer Research Foundation

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This randomized clinical trial studies the feasibility of tailored physical activity intervention that is administered using Interactive Voice Response technology and cell phones. Interactive voice response and health coach support may motivate overweight postmenopausal women to stick to their exercise regimen to reduce the risk of getting breast cancer.
Detailed Description
PRIMARY OBJECTIVES: I. To design, develop and test the feasibility of implementing a physical activity intervention using tailored communication and Interactive Voice Response (IVR) technology. We will to address four basic questions to accomplish this aim: Among overweight, postmenopausal women, who pass the screening criteria, what is the percentage of women who are willing to participate in a 12-week physical activity intervention that includes two 1-mile walk tests and two visits to the General Clinical Research Center (GCRC)? After beginning the study, what proportion of women use the cell phone and land line at least 5 days a week to get a physical activity intervention message? How many participants are enrolled and participating in the study at the end of the 12-week intervention period? On average, how many steps per day do participants walk? How many of the participants reach the 10,000 steps-per-day target by the end of the 12 week-intervention? SECONDARY OBJECTIVES: I. The effectiveness (satisfaction, convenience, ease of operation) of all the materials and processes. II. Examine whether social support from a health coach results in improvements in our measures of adherence and satisfaction. III. Examine the correlation between self-reported steps per day with improvements in performance on a 1-mile walk test administered at the beginning and the end of the 12-week intervention. OUTLINE: Patients are randomized to 1 of 2 treatment arms. ARM I. COACH-CONDITION: Participants participate in a 12-week physical activity program (walking program)and receive health mail messages via IVR system and from a health coach. Participants in this arm of the study, interacted with the IVR system and had the option of interacting with the health coach. ARM II: NO-COACH CONDITION: Participants participate in a 12-week physical activity program (walking program) administered using an IVR system.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Healthy, Obesity, Postmenopausal
Keywords
Feasibility study, Interactive voice response system (IVR), health coach, no evidence of disease

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
71 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Arm I (health coach)
Arm Type
Experimental
Arm Description
Participants participate in a 12-week physical activity intervention (walking program)and receive health mail messages via IVR system and from a health coach. Participants in this arm of the study, interacted with the IVR system and had the option of interacting with the health coach.
Arm Title
Arm II (no coach condition)
Arm Type
Active Comparator
Arm Description
Participants participate in a 12-week physical activity intervention (walking program)and receive health mail messages via IVR system. Participants in this arm of the study only interacted with the IVR system.
Intervention Type
Behavioral
Intervention Name(s)
communication intervention
Intervention Description
Participants participate in a 12-week physical activity intervention (walking program)and receive health mail messages via IVR system and had the option of communicating with a health coach.
Intervention Type
Behavioral
Intervention Name(s)
exercise intervention
Intervention Description
Participants participate in a 12-week physical activity intervention administered using an IVR system.
Primary Outcome Measure Information:
Title
Change in time taken to complete a one mile walk.
Time Frame
12 weeks
Secondary Outcome Measure Information:
Title
Changes in anthropometrics, psychometrics and the benefits of a health coach.
Time Frame
12 weeks
Title
Weekly effectiveness (satisfaction, convenience, ease of operation) of all the materials and processes as assessed by questionnaires.
Time Frame
12 weeks
Title
If the self-reported steps per day, derived from daily activity logs, relates to the change in performance on the 1-mile walk test between baseline and end of study.
Description
The steps walked per day and the change in performance on the 1-male walk test are both outcomes.
Time Frame
12 Week

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
55 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Present a letter/documentation from a primary physician stating that they can participate in a physical activity program that will require walking up to 10,000 steps per day Have a body mass index (BMI) between 25 and 40 kg/m^2 (inclusive) Be postmenopausal, defined as no period for 12 months if over age 55, or no period for 12 months; also, women who have had their ovaries removed will be considered as postmenopausal Willing to participate in a wellness program that lasts 12 weeks and involves walking for at least 30 minutes a day on most days Has access to a cell phone during the 12-week intervention Functional knowledge of English (ability to both read and write) Exclusion Criteria: Taking hormone replacement therapy within 3 months of enrollment Taking Tamoxifen or Raloxifene within 3 months of enrollment Enrolled in a weight management program, such as Weight Watchers Engaged in regular, planned walking of at least 30 minutes a day Previous history of breast cancer Premenopausal Age > 75 years, to minimize co-morbidities Cannot walk one mile
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Electra Paskett, PhD
Organizational Affiliation
Ohio State University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Ohio State University Medical Center
City
Columbus
State/Province
Ohio
ZIP/Postal Code
43210
Country
United States

12. IPD Sharing Statement

Links:
URL
http://cancer.osu.edu
Description
Jamesline

Learn more about this trial

Communication & Peer Support Effects on Physical Activity in Overweight Postmenopausal Women

We'll reach out to this number within 24 hrs