Overweight Clinical Trial
Official title:
Preliminary Trial to Evaluate the Effectiveness of the Profile by Sanford Weight Management Program in Endometrial Cancer Patients
Verified date | March 2021 |
Source | Sanford Health |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The primary purpose of this study is to evaluate the effectiveness of a 12-month comprehensive weight management program on weight change in overweight/obese patients following treatment for endometrial cancer. During the study period, subjects will be monitored for recurrence during routine clinic visits A secondary exploratory purpose of this study will be to evaluate the gut microbiome in this intervention group and the changes that may occur while participating in a weight loss and weight management program.
Status | Completed |
Enrollment | 25 |
Est. completion date | January 11, 2021 |
Est. primary completion date | January 11, 2021 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - 18 years of age and older with a diagnosis of endometrial cancer - No known metastatic disease - Has completed all treatment for their endometrial cancer at least 2 months prior to enrollment. - Has a BMI (Body Mass Index) of 30 or higher - Ability to understand the purpose of study and willingness to sign consent - Willingness to collect fecal specimens at the required time points - Capable of following the dietary guidelines and instructions for the Profile weight management plan - Agrees to sharing information between Profile and Sanford Research study personnel Exclusion Criteria: - BMI (Body Mass Index) less than 30 - Known metastatic disease - Receiving treatment or expected to receive treatment for endometrial cancer or any other cancer - Any psychological, familial, sociological conditions that the physician feels will interfere with medical follow-up and compliance on the study - Taking insulin for diabetes (oral medications for diabetes allowed) - Use of corticosteroids for a chronic medical condition - Known liver disease - Bowel or stomach disorders that the physician feels would interfere with Profile participation. - Any history of malabsorption syndrome or substantial amounts of small bowel or stomach surgery that impairs nutrient absorption |
Country | Name | City | State |
---|---|---|---|
United States | Roger Maris Cancer Center | Fargo | North Dakota |
United States | Sanford Gynecological Oncology clinic | Sioux Falls | South Dakota |
Lead Sponsor | Collaborator |
---|---|
Sanford Health |
United States,
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Linkov F, Goughnour SL, Ma T, Xu Z, Edwards RP, Lokshin AE, Ramanathan RC, Hamad GG, McCloskey C, Bovbjerg DH. Changes in inflammatory endometrial cancer risk biomarkers in individuals undergoing surgical weight loss. Gynecol Oncol. 2017 Oct;147(1):133-138. doi: 10.1016/j.ygyno.2017.07.144. Epub 2017 Aug 7. — View Citation
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McCarroll ML, Armbruster S, Pohle-Krauza RJ, Lyzen AM, Min S, Nash DW, Roulette GD, Andrews SJ, von Gruenigen VE. Feasibility of a lifestyle intervention for overweight/obese endometrial and breast cancer survivors using an interactive mobile application. Gynecol Oncol. 2015 Jun;137(3):508-15. doi: 10.1016/j.ygyno.2014.12.025. Epub 2015 Feb 11. — View Citation
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Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Determine weight change from baseline to 6 months. | All enrolled subjects will be weighed in pounds and the difference from baseline to 6 months will be recorded. | 6 months after starting weight management program | |
Primary | Determine weight change from baseline to 12 months. | All enrolled subjects will be weighed in pounds and the difference from baseline to 12 months will be recorded. | 12 months after starting weight management program |
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