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Weight Loss Referral for Healthier Survivorship in Obese Stage I-II Endometrial Cancer Survivors or Atypical Hyperplasia

Primary Purpose

Complex Endometrial Hyperplasia With Atypia, Stage IA Uterine Corpus Cancer, Stage IB Uterine Corpus Cancer

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Weight Loss Specialist
Quality-of-Life Assessment
Medical Chart Review
Sponsored by
Case Comprehensive Cancer Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Complex Endometrial Hyperplasia With Atypia

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Women with a history of stage I or II endometrial cancer or a diagnosis of complex atypical hyperplasia
  • BMI of at least 30 kg/msq

Exclusion Criteria:

  • Advanced disease (stage III or greater)
  • Recurrent or progressive endometrial cancer
  • Non endometrioid histology (such as serous uterine cancer or uterine carcinosarcoma)
  • History of bariatric surgery for weight loss
  • Ongoing medically supervised weight loss (under the care of a physician)
  • Poorly controlled psychiatric or medical conditions
  • Active second primary malignancy

Sites / Locations

  • Cleveland Clinic Taussig Cancer Institute, Case Comprehensive Cancer Center

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Weight Loss Referral

Arm Description

Patients are referred to a weight loss specialist for assistance with weight loss and medical chart reviews are performed at baseline and every 3 months for 24 months. Patients complete Quality-of-Life Assessment (EORTC- QLQ-C30 and EORTC-QLQ-EN24) at baseline, 12, and 24 months. Patients are also contacted at 90 days to determine whether they have initiated any weight loss interventions.

Outcomes

Primary Outcome Measures

Accrual with intervention, defined as number of subjects who agree to participate
Descriptive statistics will be used. Will be compared using chi square or fisher exact tests.
Compliance with intervention, defined as number of patients who follow up with the obesity referral
Descriptive statistics will be used. Will be compared using chi square or fisher exact tests.

Secondary Outcome Measures

Weight loss (in kilograms)
Descriptive statistics will be used. Will compare groups using a paired t-test.
Weight loss (in kilograms)
Descriptive statistics will be used. Will compare groups using a paired t-test.
Compliance with lifestyle changes (based on affirmative response to 3 month follow up when asked if lifestyle changes have been adopted)
Will be compared using chi square or fisher exact tests.
Incidence of obesity related comorbidities and adverse events (diabetes, hypertension, myocardial infarction, stroke, venous thromboembolism)
Descriptive statistics will be used to detail incidence of new major health events (myocardial infarction, stroke, new diabetes diagnosis, new venous thromboembolism, new hypertension diagnosis, death, date of death, cause of death). The occurrence new major health events and cancer related events will be compared using chi square or fisher exact tests.
Incidence of obesity related comorbidities and adverse events (diabetes, hypertension, myocardial infarction, stroke, venous thromboembolism)
Descriptive statistics will be used to detail incidence of new major health events (myocardial infarction, stroke, new diabetes diagnosis, new venous thromboembolism, new hypertension diagnosis, death, date of death, cause of death). The occurrence new major health events and cancer related events will be compared using chi square or fisher exact tests.
Incidence of obesity related comorbidities and adverse events (diabetes, hypertension, myocardial infarction, stroke, venous thromboembolism)
Descriptive statistics will be used to detail incidence of new major health events (myocardial infarction, stroke, new diabetes diagnosis, new venous thromboembolism, new hypertension diagnosis, death, date of death, cause of death). The occurrence new major health events and cancer related events will be compared using chi square or fisher exact tests.
Progression free survival
Descriptive statistics will be used. Will be described with Kaplan Meier curves.
Overall survival
Descriptive statistics will be used. Will be described with Kaplan Meier curves.
Recurrence rate
Descriptive statistics will be used to detail cancer related outcomes (cancer recurrence, date and location of recurrence, cancer related death).
Level of functioning, quality of life, and symptomatology, as measured by the EORTC-QLQ-C30 and EORTC-QLQ-EN24
Will compare groups using a paired t-test.
Level of functioning, quality of life, and symptomatology, as measured by the EORTC-QLQ-C30 and EORTC-QLQ-EN24
Will compare groups using a paired t-test.

Full Information

First Posted
January 15, 2015
Last Updated
November 15, 2018
Sponsor
Case Comprehensive Cancer Center
Collaborators
National Cancer Institute (NCI)
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1. Study Identification

Unique Protocol Identification Number
NCT02342730
Brief Title
Weight Loss Referral for Healthier Survivorship in Obese Stage I-II Endometrial Cancer Survivors or Atypical Hyperplasia
Official Title
Referral of Obese Endometrial Cancer Survivors to a Bariatric Specialist and a Healthier Survivorship: A Prospective Intervention Cohort Study
Study Type
Interventional

2. Study Status

Record Verification Date
November 2018
Overall Recruitment Status
Completed
Study Start Date
December 17, 2014 (undefined)
Primary Completion Date
May 18, 2015 (Actual)
Study Completion Date
May 18, 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Case Comprehensive Cancer Center
Collaborators
National Cancer Institute (NCI)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This pilot clinical trial studies whether obese stage I-II endometrial cancer survivors or patients with atypical hyperplasia (abnormal cells in the lining of the uterus) would go see a weight loss specialist if it was recommended by their cancer doctor. Excess body weight or obesity is one of the most common contributors to (causes of) endometrial cancer. Over two-thirds of women who have survived endometrial cancer are obese. Complications of obesity, such as heart disease are often more dangerous than the cancer itself. A weight loss of even 5-10% of excess body weight is associated with improved health. Often, meeting with a doctor or person who is an expert in weight loss (bariatric specialist) is the best way to lose weight and keep it off. Endometrial cancer survivors or patients with atypical hyperplasia who go see a weight loss specialist recommended by their doctor may be able to achieve a healthier body weight.
Detailed Description
PRIMARY OBJECTIVES: I.Our primary outcome for the purposes of the pilot study will be to describe recruitment in terms of accrual (number of subjects who agree to participate) and compliance (number of patients who follow up with the obesity referral). This will be described in terms of a specific number as well as a rate. Accrual rate is the number of women accrued divided by the number of women approached for the study. Compliance rate is the number of women who comply with the referral divided by the number of women accrued. Several secondary outcomes will be described: Weight loss at 12 & 24 months. Obesity interventions implemented (medical, surgical, behavioral, and selfguided) The incidence of obesity related comorbidities at baseline and 12 and 24 months (myocardial infarction, venous thromboembolism, stroke, diabetes and hypertension.) Cancer specific outcomes (recurrence rate, progression free survival). Mortality otucomes (Overall survival, cause of death) In patients with diabetes, we will record the number of diabetic medications required and the most recent hemoglobin A1C. In patients with hypertension, we will record the number of antihypertensive medications required We will assess the level of functioning, quality of life and symptomatology of women at baseline, 12 and 24 months using the EORTC-QLQ-C30 and EORTC-QLQ-EN24. Primary and secondary outcomes will be compared in relation to the timing of the referral by the gynecologic oncologist (within 1 year or greater than 1 year out from the endometrial cancer/hyperplasia diagnosis). Secondary outcomes of subjects included in this study will be compared to a historic cohort matches for age, stage and BMI in a 2:1 fashion. OUTLINE: Patients are referred to a weight loss specialist for assistance with weight loss and chart reviews are performed at baseline and every 3 months for 24 months. Patients complete the European Organization for Research and Treatment of Cancer (EORTC)-Quality of Life Questionnaire (QLQ)-Cancer (C)30 and EORTC-QLQ-Endometrial Cancer (EN)24 at baseline, 12, and 24 months. Patients are also contacted at 90 days to determine whether they have initiated any weight loss interventions.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Complex Endometrial Hyperplasia With Atypia, Stage IA Uterine Corpus Cancer, Stage IB Uterine Corpus Cancer, Stage II Uterine Corpus Cancer

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
127 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Weight Loss Referral
Arm Type
Experimental
Arm Description
Patients are referred to a weight loss specialist for assistance with weight loss and medical chart reviews are performed at baseline and every 3 months for 24 months. Patients complete Quality-of-Life Assessment (EORTC- QLQ-C30 and EORTC-QLQ-EN24) at baseline, 12, and 24 months. Patients are also contacted at 90 days to determine whether they have initiated any weight loss interventions.
Intervention Type
Behavioral
Intervention Name(s)
Weight Loss Specialist
Other Intervention Name(s)
Behavior Conditioning Therapy, Behavior Modification, Behavior or Life Style Modifications, Behavior Therapy, Behavioral Interventions, Behavioral Intervention
Intervention Description
Referred to a weight loss specialist
Intervention Type
Other
Intervention Name(s)
Quality-of-Life Assessment
Other Intervention Name(s)
Quality of Life Assessment
Intervention Description
Complete EORTC-QLQ questionnaires
Intervention Type
Other
Intervention Name(s)
Medical Chart Review
Other Intervention Name(s)
Chart Review
Intervention Description
Chart reviews are performed
Primary Outcome Measure Information:
Title
Accrual with intervention, defined as number of subjects who agree to participate
Description
Descriptive statistics will be used. Will be compared using chi square or fisher exact tests.
Time Frame
Up to 24 months
Title
Compliance with intervention, defined as number of patients who follow up with the obesity referral
Description
Descriptive statistics will be used. Will be compared using chi square or fisher exact tests.
Time Frame
Up to 24 months
Secondary Outcome Measure Information:
Title
Weight loss (in kilograms)
Description
Descriptive statistics will be used. Will compare groups using a paired t-test.
Time Frame
Baseline to 12 months
Title
Weight loss (in kilograms)
Description
Descriptive statistics will be used. Will compare groups using a paired t-test.
Time Frame
Baseline to 24 months
Title
Compliance with lifestyle changes (based on affirmative response to 3 month follow up when asked if lifestyle changes have been adopted)
Description
Will be compared using chi square or fisher exact tests.
Time Frame
At 3 months
Title
Incidence of obesity related comorbidities and adverse events (diabetes, hypertension, myocardial infarction, stroke, venous thromboembolism)
Description
Descriptive statistics will be used to detail incidence of new major health events (myocardial infarction, stroke, new diabetes diagnosis, new venous thromboembolism, new hypertension diagnosis, death, date of death, cause of death). The occurrence new major health events and cancer related events will be compared using chi square or fisher exact tests.
Time Frame
Baseline
Title
Incidence of obesity related comorbidities and adverse events (diabetes, hypertension, myocardial infarction, stroke, venous thromboembolism)
Description
Descriptive statistics will be used to detail incidence of new major health events (myocardial infarction, stroke, new diabetes diagnosis, new venous thromboembolism, new hypertension diagnosis, death, date of death, cause of death). The occurrence new major health events and cancer related events will be compared using chi square or fisher exact tests.
Time Frame
At 12 months
Title
Incidence of obesity related comorbidities and adverse events (diabetes, hypertension, myocardial infarction, stroke, venous thromboembolism)
Description
Descriptive statistics will be used to detail incidence of new major health events (myocardial infarction, stroke, new diabetes diagnosis, new venous thromboembolism, new hypertension diagnosis, death, date of death, cause of death). The occurrence new major health events and cancer related events will be compared using chi square or fisher exact tests.
Time Frame
At 24 months
Title
Progression free survival
Description
Descriptive statistics will be used. Will be described with Kaplan Meier curves.
Time Frame
Up to 24 months
Title
Overall survival
Description
Descriptive statistics will be used. Will be described with Kaplan Meier curves.
Time Frame
Up to 24 months
Title
Recurrence rate
Description
Descriptive statistics will be used to detail cancer related outcomes (cancer recurrence, date and location of recurrence, cancer related death).
Time Frame
Up to 24 months
Title
Level of functioning, quality of life, and symptomatology, as measured by the EORTC-QLQ-C30 and EORTC-QLQ-EN24
Description
Will compare groups using a paired t-test.
Time Frame
At 12 months
Title
Level of functioning, quality of life, and symptomatology, as measured by the EORTC-QLQ-C30 and EORTC-QLQ-EN24
Description
Will compare groups using a paired t-test.
Time Frame
At 24 months

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Women with a history of stage I or II endometrial cancer or a diagnosis of complex atypical hyperplasia BMI of at least 30 kg/msq Exclusion Criteria: Advanced disease (stage III or greater) Recurrent or progressive endometrial cancer Non endometrioid histology (such as serous uterine cancer or uterine carcinosarcoma) History of bariatric surgery for weight loss Ongoing medically supervised weight loss (under the care of a physician) Poorly controlled psychiatric or medical conditions Active second primary malignancy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Amelia Jernigan
Organizational Affiliation
Case Comprehensive Cancer Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Cleveland Clinic Taussig Cancer Institute, Case Comprehensive Cancer Center
City
Cleveland
State/Province
Ohio
ZIP/Postal Code
44195
Country
United States

12. IPD Sharing Statement

Learn more about this trial

Weight Loss Referral for Healthier Survivorship in Obese Stage I-II Endometrial Cancer Survivors or Atypical Hyperplasia

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