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Rural Women Connecting for Better Health

Primary Purpose

Breast Cancer, Obesity

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Group phone counseling
Newsletter
Sponsored by
University of Kansas Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Breast Cancer focused on measuring weight loss, breast cancer, obesity, overweight, rural women, community based, Secondary Prevention

Eligibility Criteria

undefined - 75 Years (Child, Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Breast cancer patients with a BMI 27-45 kg/m2
  • Diagnosis of Stage 0-IIIc disease within the past 10 years (except Stage 0, treated with mastectomy only)
  • Have completed all local and systemic therapy at least 3 months prior to entry
  • Have clearance from their oncologist or current medical provider to participate in a weight control study
  • Must be ≤ 75 years old
  • Post-menopausal
  • Participants must live in a rural area
  • Have access to a phone
  • Able to participate in the physical activity component of the intervention, i.e., be able to walk briskly unassisted and without serious medical risk
  • Weight stable within ten pounds three months prior to entry

Exclusion Criteria:

  • Women with insulin-dependent diabetes
  • Ongoing participation in a formal weight loss program
  • Ongoing use of pharmacotherapy for weight loss
  • Ongoing use of medications that seriously affect weight and metabolism (e.g., steroids, phentermine)
  • Positive screen for current substance abuse, major depression, or binge eating disorder
  • Any cardiac or pulmonary disease preventing participation
  • Treatment for any other cancers within the past year
  • Previous bariatric surgery

Sites / Locations

  • University of Kansas Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Group (GRP) phone counseling

Mail-based Comparison Condition

Arm Description

The group phone counseling includes 26 bi-weekly phone sessions from 6 to 18 months and focuses on group problem-solving. Women continue in the same group as in weight loss intervention phase.

Participants in this group will receive a newsletter by mail every other week for 12 months starting after the initial 6 month weight loss period. The newsletters will provide problem-solving tips and will review nutrition and physical activity information.

Outcomes

Primary Outcome Measures

Weight loss maintenance
Examine the impact of group phone-based treatment on weight loss maintenance from 6 to 18 months, compared to a mail-based education COMPARISON condition, following a 6-month weight loss phase among obese rural breast cancer survivors.

Secondary Outcome Measures

Quality of life
Compare the effects of treatment conditions on aspects of quality of life important for breast cancer survivorship, including general physical, social, and emotional well-being, fatigue, arthralgia, lymphedema symptoms, menopausal symptoms, and depressive symptoms.
Breast cancer risk biomarkers
Examine the association of weight change with changes in selected breast cancer risk biomarkers, including bioavailable estradiol, testosterone, and fasting insulin. Examine whether modulation of biomarkers is sustained during weight loss maintenance.
Cost effectiveness
Compare the incremental cost-effectiveness of weight loss maintenance (kg below baseline) between group and control conditions. Costs include fixed and variable provider costs (facility, time, phone charges, supplies) and fixed and variable participant costs (time, out-of-pocket expenses).

Full Information

First Posted
September 23, 2011
Last Updated
November 22, 2016
Sponsor
University of Kansas Medical Center
Collaborators
National Cancer Institute (NCI)
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1. Study Identification

Unique Protocol Identification Number
NCT01441011
Brief Title
Rural Women Connecting for Better Health
Official Title
Group Phone-Based Weight Control for Rural Breast Cancer Survivors
Study Type
Interventional

2. Study Status

Record Verification Date
November 2016
Overall Recruitment Status
Completed
Study Start Date
August 2011 (undefined)
Primary Completion Date
April 2015 (Actual)
Study Completion Date
October 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Kansas Medical Center
Collaborators
National Cancer Institute (NCI)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Women who are obese at breast cancer diagnosis have a 1.5 to 2.5 increased risk of recurrence and death compared to their normal weight counterparts. Moreover, weight gain and decreased physical activity are common after diagnosis and also increase the likelihood of breast cancer recurrence and death. Rural women suffer from health disparities in breast cancer diagnosis and treatment. Women of the most rural counties also have the highest prevalence of obesity compared to urban women. To address these disparities, the overarching objective of this proposal is to develop a clinically effective and cost efficient strategy for delivering a weight control intervention to rural breast cancer survivors. Group phone-based treatment via conference call is a novel treatment delivery approach that the investigators have shown to be effective for initial weight loss among rural breast cancer survivors and more effective than the standard individual phone-based approach among rural women. This innovative method of providing group treatment addresses access barriers in rural areas and may be especially ideal for rural breast cancer survivors because it provides social support in conjunction with a level of anonymity. However, the impact of group phone counseling during extended care for weight loss maintenance beyond 6 months remains unknown. Weight loss maintenance is the more challenging phase of treatment when weight regain is common, and this regain presents a potential risk for breast cancer recurrence. This randomized controlled trial will evaluate the effects of group phone-based treatment for weight loss maintenance among rural breast cancer survivors, compared to an established mail-based education comparison condition, subsequent to a 6 month group phone-based weight loss phase for both conditions. In addition to the intervention impact on weight loss maintenance, the study will provide estimates of incremental cost-effectiveness per kg loss between the two conditions and the impact on secondary outcomes including quality of life, breast cancer risk biomarkers, dietary intake, and physical activity.
Detailed Description
Phase 1 - Weight Loss (0-6 months) Weekly group phone counseling sessions for all participants (12-14 women per group) via conference call for 26 consecutive weeks Low-calorie, low-fat diet recommended, including 2 pre-packaged entrees, five one-cup servings of fruits and vegetables and meal replacement shakes (provided free of charge) Physical activity program program recommended, beginning with 15 minutes per day, 3 days a week, working toward a goal of 225 minutes a week Experienced group counselor facilitates all sessions Phase 2 - Weight Loss Maintenance (6-18 months) Participants randomized to either group phone counseling or mail-based comparison with no phone counseling Weight loss maintenance group condition includes 26 bi-weekly phone sessions, while mail-based comparison includes 26 bi-weekly newsletters in the mail Focus is on problem-solving Phase 3 - Transition to Self-Reliance (18-24 months) Lasts from 18-24 months No sessions or newsletter mailings Participants are encouraged to continue to self-monitor throughout this period

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Cancer, Obesity
Keywords
weight loss, breast cancer, obesity, overweight, rural women, community based, Secondary Prevention

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Group (GRP) phone counseling
Arm Type
Experimental
Arm Description
The group phone counseling includes 26 bi-weekly phone sessions from 6 to 18 months and focuses on group problem-solving. Women continue in the same group as in weight loss intervention phase.
Arm Title
Mail-based Comparison Condition
Arm Type
Active Comparator
Arm Description
Participants in this group will receive a newsletter by mail every other week for 12 months starting after the initial 6 month weight loss period. The newsletters will provide problem-solving tips and will review nutrition and physical activity information.
Intervention Type
Behavioral
Intervention Name(s)
Group phone counseling
Intervention Description
Bi-weekly phone counseling sessions from 6 - 18 months
Intervention Type
Behavioral
Intervention Name(s)
Newsletter
Intervention Description
Bi-weekly newsletter mailings from 6 - 18 months
Primary Outcome Measure Information:
Title
Weight loss maintenance
Description
Examine the impact of group phone-based treatment on weight loss maintenance from 6 to 18 months, compared to a mail-based education COMPARISON condition, following a 6-month weight loss phase among obese rural breast cancer survivors.
Time Frame
6 - 18 months
Secondary Outcome Measure Information:
Title
Quality of life
Description
Compare the effects of treatment conditions on aspects of quality of life important for breast cancer survivorship, including general physical, social, and emotional well-being, fatigue, arthralgia, lymphedema symptoms, menopausal symptoms, and depressive symptoms.
Time Frame
Baseline and 6, 12, 18, and 24 months
Title
Breast cancer risk biomarkers
Description
Examine the association of weight change with changes in selected breast cancer risk biomarkers, including bioavailable estradiol, testosterone, and fasting insulin. Examine whether modulation of biomarkers is sustained during weight loss maintenance.
Time Frame
Baseline and 6 and 18 months
Title
Cost effectiveness
Description
Compare the incremental cost-effectiveness of weight loss maintenance (kg below baseline) between group and control conditions. Costs include fixed and variable provider costs (facility, time, phone charges, supplies) and fixed and variable participant costs (time, out-of-pocket expenses).
Time Frame
18 months

10. Eligibility

Sex
Female
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Breast cancer patients with a BMI 27-45 kg/m2 Diagnosis of Stage 0-IIIc disease within the past 10 years (except Stage 0, treated with mastectomy only) Have completed all local and systemic therapy at least 3 months prior to entry Have clearance from their oncologist or current medical provider to participate in a weight control study Must be ≤ 75 years old Post-menopausal Participants must live in a rural area Have access to a phone Able to participate in the physical activity component of the intervention, i.e., be able to walk briskly unassisted and without serious medical risk Weight stable within ten pounds three months prior to entry Exclusion Criteria: Women with insulin-dependent diabetes Ongoing participation in a formal weight loss program Ongoing use of pharmacotherapy for weight loss Ongoing use of medications that seriously affect weight and metabolism (e.g., steroids, phentermine) Positive screen for current substance abuse, major depression, or binge eating disorder Any cardiac or pulmonary disease preventing participation Treatment for any other cancers within the past year Previous bariatric surgery
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Christie Befort, Ph.D.
Organizational Affiliation
University of Kansas Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Kansas Medical Center
City
Kansas City
State/Province
Kansas
ZIP/Postal Code
66160
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
29086523
Citation
Fazzino TL, Fabian C, Befort CA. Change in Physical Activity During a Weight Management Intervention for Breast Cancer Survivors: Association with Weight Outcomes. Obesity (Silver Spring). 2017 Nov;25 Suppl 2(Suppl 2):S109-S115. doi: 10.1002/oby.22007.
Results Reference
derived
PubMed Identifier
28410181
Citation
Fazzino TL, Fleming K, Befort C. Alcohol Intake Among Breast Cancer Survivors: Change in Alcohol Use During a Weight Management Intervention. JMIR Cancer. 2016 Nov 9;2(2):e15. doi: 10.2196/cancer.6295.
Results Reference
derived
PubMed Identifier
26932848
Citation
Fazzino TL, Sporn NJ, Befort CA. A qualitative evaluation of a group phone-based weight loss intervention for rural breast cancer survivors: Themes and mechanisms of success. Support Care Cancer. 2016 Jul;24(7):3165-73. doi: 10.1007/s00520-016-3149-7. Epub 2016 Mar 2.
Results Reference
derived
PubMed Identifier
24486636
Citation
Befort CA, Klemp JR, Fabian C, Perri MG, Sullivan DK, Schmitz KH, Diaz FJ, Shireman T. Protocol and recruitment results from a randomized controlled trial comparing group phone-based versus newsletter interventions for weight loss maintenance among rural breast cancer survivors. Contemp Clin Trials. 2014 Mar;37(2):261-71. doi: 10.1016/j.cct.2014.01.010. Epub 2014 Jan 31.
Results Reference
derived
Links:
URL
http://cancercontrol.cancer.gov/ocs/index.html
Description
National Cancer Institute: Cancer Survivorship Research

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Rural Women Connecting for Better Health

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