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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03908996
Other study ID # SH Profile II
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 11, 2019
Est. completion date January 11, 2021

Study information

Verified date March 2021
Source Sanford Health
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Description:

All enrolled subjects will participate in the Profile weight loss and weight management program for a period of 12 months. They will work with a Profile lifestyle coach weekly to develop a personalized nutrition plan, discuss their activity, and lifestyle behavior as done with all Profile members. A comparison of similar retrospective chart reviews based on age, weight in pounds and stage of cancer will be conducted using the Electronic Medical Record (EMR). All enrolled subjects will collect and return a fecal specimen prior to beginning the weight management plan and again after 6 months of participation. The stool sample will be used to understand gut health.


Recruitment information / eligibility

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

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Profile by Sanford weight management plan
The purpose of this study is to observe weight changes in patients who completed endometrial cancer treatment, are clinically overweight, and who participate in the Profile by Sanford weight management program. An exploratory purpose is to examine the bacterial content of the patient's gut by examining stool specimens before starting the Profile by Sanford weight management program and after 6 months of participation in the Profile by Sanford weight management program.

Locations

Country Name City State
United States Roger Maris Cancer Center Fargo North Dakota
United States Sanford Gynecological Oncology clinic Sioux Falls South Dakota

Sponsors (1)

Lead Sponsor Collaborator
Sanford Health

Country where clinical trial is conducted

United States, 

References & Publications (9)

Hoedjes M, van Stralen MM, Joe STA, Rookus M, van Leeuwen F, Michie S, Seidell JC, Kampman E. Toward the optimal strategy for sustained weight loss in overweight cancer survivors: a systematic review of the literature. J Cancer Surviv. 2017 Jun;11(3):360-385. doi: 10.1007/s11764-016-0594-8. Epub 2017 Jan 18. Review. — View Citation

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

Luo J, Hendryx M, Chlebowski RT. Intentional weight loss and cancer risk. Oncotarget. 2017 Sep 6;8(47):81719-81720. doi: 10.18632/oncotarget.20671. eCollection 2017 Oct 10. — View Citation

Massetti GM, Dietz WH, Richardson LC. Excessive Weight Gain, Obesity, and Cancer: Opportunities for Clinical Intervention. JAMA. 2017 Nov 28;318(20):1975-1976. doi: 10.1001/jama.2017.15519. — View Citation

McCarroll ML, Armbruster S, Frasure HE, Gothard MD, Gil KM, Kavanagh MB, Waggoner S, von Gruenigen VE. Self-efficacy, quality of life, and weight loss in overweight/obese endometrial cancer survivors (SUCCEED): a randomized controlled trial. Gynecol Oncol. 2014 Feb;132(2):397-402. doi: 10.1016/j.ygyno.2013.12.023. Epub 2013 Dec 22. — View Citation

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

Steele CB, Thomas CC, Henley SJ, Massetti GM, Galuska DA, Agurs-Collins T, Puckett M, Richardson LC. Vital Signs: Trends in Incidence of Cancers Associated with Overweight and Obesity - United States, 2005-2014. MMWR Morb Mortal Wkly Rep. 2017 Oct 3;66(39):1052-1058. doi: 10.15585/mmwr.mm6639e1. — View Citation

Yu J, Feng Q, Wong SH, Zhang D, Liang QY, Qin Y, Tang L, Zhao H, Stenvang J, Li Y, Wang X, Xu X, Chen N, Wu WK, Al-Aama J, Nielsen HJ, Kiilerich P, Jensen BA, Yau TO, Lan Z, Jia H, Li J, Xiao L, Lam TY, Ng SC, Cheng AS, Wong VW, Chan FK, Xu X, Yang H, Madsen L, Datz C, Tilg H, Wang J, Brünner N, Kristiansen K, Arumugam M, Sung JJ, Wang J. Metagenomic analysis of faecal microbiome as a tool towards targeted non-invasive biomarkers for colorectal cancer. Gut. 2017 Jan;66(1):70-78. doi: 10.1136/gutjnl-2015-309800. Epub 2015 Sep 25. — View Citation

Zitvogel L, Ma Y, Raoult D, Kroemer G, Gajewski TF. The microbiome in cancer immunotherapy: Diagnostic tools and therapeutic strategies. Science. 2018 Mar 23;359(6382):1366-1370. doi: 10.1126/science.aar6918. Review. — View Citation

Outcome

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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