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Time-Restricted Eating and Mindfulness-Based Stress Reduction to Reduce the Risk of Early-Onset Colorectal Cancer (MBSR&TRE)

Primary Purpose

Obesity, Colorectal Cancer, Microbial Colonization

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
TRE
MBSR
Sponsored by
Lisa Tussing-Humphreys
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Obesity focused on measuring obesity; Time Restricted Feeding; microbiome; chronic stress

Eligibility Criteria

18 Years - 39 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: 18-39 years old. BMI 30-49.99 kg/m2. Own and use a smartphone, computer, or tablet with access to the Internet. Score ≥ 14 on the Perceived Stress Score (PSS) at screening. Exclusion Criteria: Have a personal or family history of EOCRC. Have taken antibiotics in the previous 2 months. Have an inflammatory bowel disease or genetic predisposition to EOCRC or CRC (e.g., Lynch syndrome);. Any cancer diagnosis or cancer treatment in the past 12 months. Consume >50 grams ethanol daily (approximately 4-5, 12 ounces beers). Use combustible tobacco. Have history of bariatric surgery or bowel resection. Have an active infection. Have type 1 or type 2 diabetes, immunodeficiency/autoimmune disorder, or inflammatory bowel disease. Use fiber or pre-/probiotic supplements >3 days per week. Currently taking corticosteroids medication - inhaled, topical, or oral in the past 2 months (affects cortisol measures). Are on a weight-loss diet or involved in a formal weight-loss program or are not weight stable for 3 months (+/- 4.5 kg) prior to the study. Females who are pregnant/trying to become pregnant. Have schizophrenia (medication can affect study outcomes). Have an eating window of <10 hours/day or are currently following an intermittent fasting pattern. Night shift workers (shift passes midnight). Present a history of eating disorder. Currently taking weight loss medication. Illegal drug use in the past month (not marijuana).

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm 3

    Arm 4

    Arm Type

    Experimental

    Experimental

    Experimental

    No Intervention

    Arm Label

    TRE alone

    MBSR alone

    TRE + MBSR

    Control

    Arm Description

    Participants will be instructed to eat ad libitum from noon - 8:00pm daily and fast from 8:00pm - noon (16-h fast) for 8 weeks. During the 8-h eating window, there will be no restrictions on types or quantities of foods consumed. Participants will meet with a registered dietitian (RD) for 30 minutes at the start of the intervention to review instructions and goals and weekly thereafter. Adherence to the TRE intervention will be assessed as the number of adherent days per week.

    Participants in this study will be granted access to a remote mindfulness-based stress reductions (MBSR) protocol. Participants will have access to the MBSR course, consisting of 30 audio lessons, each ranging from 9 to 14 minutes long. During the study, participants will be asked to complete four lessons per week during weeks 1-7 and two lessons during week 8.

    This group will follow a combined protocol of the TRE and MBSR interventions as described above.

    The control group will not receive any of the interventions previously described. To maintain a relationship with each participant in the control group, we will contact them once a week via text message to engage them to finalize the intervention period. At the end of the intervention period and after all data is collected, the RD will meet with the participant for 30 minutes and will educate them regarding the TRE protocol and provide access to the MBSR web-based program.

    Outcomes

    Primary Outcome Measures

    Feasibility of the study
    the number of people interested in the study, those who pass phone and in-person screenings, and those who decline enrollment and their reasons. Once enrolled, we will closely monitor attendance, data completeness, session attendance, asynchronous intervention usage, and loss to follow-up/withdrawal. To monitor participant progress, we will update the CONSORT participant flow diagram every week. Participants who withdraw voluntarily will be asked for their reasons.
    Acceptability of the study
    Participants will complete the acceptability of intervention measure (scores range from 4-20 points with higher scores reflecting higher acceptability).

    Secondary Outcome Measures

    Hair cortisol
    Objective stress markers will be measured via hair cortisol
    Serum adrenocorticotropic hormone (ACTH)
    Objective stress markers will be measured via serum ACTH.
    Serum cortisol
    Objective stress markers will be measured via serum cortisol.
    Serum norepinephrine
    Objective stress markers will be measured via serum norepinephrine
    Perceived Stress Scale.
    The Perceived Stress Scale queries participants' perceptions of feeling stress during the last month. Responses were on a 5-point scale from "never" to "very often." Scores will be summed to indicate current stress levels, with higher scores suggesting greater perceived stress (≥ 14 indicates moderate to high perceived stress).
    Body fat mass
    Body fat mass will be measured via whole body dual energy x-ray absorptiometry (DEXA) scan.
    Body lean mass
    Body lean mass will be measured via whole body dual energy x-ray absorptiometry (DEXA) scan.
    Body bone density
    Body bone density will be measured via whole body dual energy x-ray absorptiometry (DEXA) scan.
    Triglycerides
    Will be measured from plasma by a commercial lab.
    High sensitivity C-reactive protein.
    Will be measured from plasma by a commercial lab.
    homeostasis model assessment-insulin resistance (HOMA-IR)
    calculated from fasting glucose and insulin using a standard formula.
    Microbial Deoxyribonucleic acid (DNA) isolation: 16S on V4 region
    performed on stool using Microbial DNA isolation

    Full Information

    First Posted
    August 23, 2023
    Last Updated
    September 1, 2023
    Sponsor
    Lisa Tussing-Humphreys
    Collaborators
    University of Illinois at Chicago
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    1. Study Identification

    Unique Protocol Identification Number
    NCT06022887
    Brief Title
    Time-Restricted Eating and Mindfulness-Based Stress Reduction to Reduce the Risk of Early-Onset Colorectal Cancer
    Acronym
    MBSR&TRE
    Official Title
    Feasibility and Acceptability of a Remote Time-Restricted Eating and Mindfulness-Based Stress Reduction Intervention to Reduce Risk Factors Associated With Early-Onset Colorectal Cancer Development Among Young Adults
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    August 2023
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    September 2023 (Anticipated)
    Primary Completion Date
    May 2024 (Anticipated)
    Study Completion Date
    May 2024 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor-Investigator
    Name of the Sponsor
    Lisa Tussing-Humphreys
    Collaborators
    University of Illinois at Chicago

    4. Oversight

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

    5. Study Description

    Brief Summary
    The goal of this clinical trial is to evaluate the feasibility of remote time-restricted eating (TRE) and mindfulness-based stress reduction (MBSR) interventions and the preliminary effect on EOCRC-related markers. The main question[s] it aims to answer are: Is it feasible and acceptable to conduct 8-week remote interventions of TRE, MBSR, and combined TRE+MBSR among young adults with excess adiposity and moderate-to-severe perceived stress? Will participants in the combined group lose more body weight and reduce their stress levels than those in the remaining groups? Will participants in the combined group experience better body composition changes and improve their cardiometabolic health compared to those in the remaining groups? Will participants in the combined group exhibit changes in the microbiome compared to those in the remaining groups? Participants will: Complete 8 weeks of a TRE intervention Complete 8 weeks of a remote MBSR intervention Researchers will compare 1. TRE alone; 2. MBSR alone; 3. TRE + MBSR; and 4. Control to see if the study is feasible and acceptable; to see if individuals lose body weight; to see if individual stress levels reduce; to see changes in the microbiome.
    Detailed Description
    Early onset colorectal cancer (EOCRC) is defined as a diagnosis of colorectal cancer (CRC) in patients younger than 50 years old. The American Cancer Society reported that 12% of all CRC diagnoses as occurring in individuals younger than 50 years old. Worldwide, a steady increase in EOCRC cases is observed among Westernized countries, which suggests that similar risk factors and exposures within these developed countries are contributors to EOCRC. In particular, increased adiposity from an early age that persists through adulthood and chronic psychosocial stress are under investigation as drivers of the recent uptick in EOCRC in the United States (US) and other Westernized countries. Obesity in early adulthood is strongly associated with increased risk of EOCRC; in the US, obesity affects 42% of adults. In addition, obesity is associated with metabolic, hormonal, and immune perturbations that can promote gene mutations that drive EOCRC tumorigenesis. Chronic stress can negatively impact several different systems of the human body including the sympathetic nervous system (SNS)-related catecholamines, epinephrine and norepinephrine, and hypothalamic-pituitary-adrenal (HPA)-axis related hormones including adrenocorticotropic hormone and the glucocorticoid, cortisol. Due to the broad impact that exposure to chronic stress has in the human body, chronic stress has been linked to several diseases, including cancer. The gut and the brain are connected through a bidirectional system coined the gut-microbiota-brain axis (GMBA). Chronic stress can disrupt the SNS, HPA-axis and immune system, leading to a shift in gut microbial ecology and metabolic function that tips the balance to a more pro-inflammatory colonic state conducive to the formation of EOCRC. This study will examine if mitigating chronic stress and weight loss can modify EOCRC risk in young adults at risk of EOCRC. Accumulating evidence suggests that time-restricted eating (TRE), a type of intermittent fasting, produces a ~300-500 kcal/d energy deficit by limiting an individual's daily eating window to 4-8 hours each day. Mindfulness meditation is the practice of cultivating a moment-to-moment awareness of internal and external experience in an accepting and open manner. In 1990, Kabat-Zinn developed Mindfulness Based Stress Reduction (MBSR): an intervention with a goal of reducing stress, pain, and suffering. MBSR is associated with lower perceived stress and decreased circulating cortisol concentrations. Existing evidence suggests that MBSR also yields EOCRC preventive effects specific to body weight reduction, increase of insulin sensitivity and reduction of inflammation. We propose to conduct an 8-week 4-arm randomized-controlled study of 1. TRE alone; 2. MBSR alone; 3. TRE + MBSR; and 4. Control among 40 young adults with obesity (BMI ≥ 30 kg/m2) and moderate to severe perceived stress (Perceived Stress Score ≥14) to evaluate the feasibility of the interventions and preliminary effect on EOCRC-related markers. Data generated from this preliminary trial would serve in developing a fully powered efficacy trial testing TRE+MBSR for EOCRC prevention among young adults in the Chicagoland area.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Obesity, Colorectal Cancer, Microbial Colonization, Time Restricted Feeding, Stress, Psychological
    Keywords
    obesity; Time Restricted Feeding; microbiome; chronic stress

    7. Study Design

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

    8. Arms, Groups, and Interventions

    Arm Title
    TRE alone
    Arm Type
    Experimental
    Arm Description
    Participants will be instructed to eat ad libitum from noon - 8:00pm daily and fast from 8:00pm - noon (16-h fast) for 8 weeks. During the 8-h eating window, there will be no restrictions on types or quantities of foods consumed. Participants will meet with a registered dietitian (RD) for 30 minutes at the start of the intervention to review instructions and goals and weekly thereafter. Adherence to the TRE intervention will be assessed as the number of adherent days per week.
    Arm Title
    MBSR alone
    Arm Type
    Experimental
    Arm Description
    Participants in this study will be granted access to a remote mindfulness-based stress reductions (MBSR) protocol. Participants will have access to the MBSR course, consisting of 30 audio lessons, each ranging from 9 to 14 minutes long. During the study, participants will be asked to complete four lessons per week during weeks 1-7 and two lessons during week 8.
    Arm Title
    TRE + MBSR
    Arm Type
    Experimental
    Arm Description
    This group will follow a combined protocol of the TRE and MBSR interventions as described above.
    Arm Title
    Control
    Arm Type
    No Intervention
    Arm Description
    The control group will not receive any of the interventions previously described. To maintain a relationship with each participant in the control group, we will contact them once a week via text message to engage them to finalize the intervention period. At the end of the intervention period and after all data is collected, the RD will meet with the participant for 30 minutes and will educate them regarding the TRE protocol and provide access to the MBSR web-based program.
    Intervention Type
    Behavioral
    Intervention Name(s)
    TRE
    Intervention Description
    daily ad libitum food intake, 8-h 12pm - 8pm, 8 wks active weight loss phase;
    Intervention Type
    Behavioral
    Intervention Name(s)
    MBSR
    Intervention Description
    Completed 30 sessions of a Mindfulness-Based Stress Reduction (MBSR) interventions for 8 weeks
    Primary Outcome Measure Information:
    Title
    Feasibility of the study
    Description
    the number of people interested in the study, those who pass phone and in-person screenings, and those who decline enrollment and their reasons. Once enrolled, we will closely monitor attendance, data completeness, session attendance, asynchronous intervention usage, and loss to follow-up/withdrawal. To monitor participant progress, we will update the CONSORT participant flow diagram every week. Participants who withdraw voluntarily will be asked for their reasons.
    Time Frame
    Baseline; through study completion, an average of 9 weeks
    Title
    Acceptability of the study
    Description
    Participants will complete the acceptability of intervention measure (scores range from 4-20 points with higher scores reflecting higher acceptability).
    Time Frame
    Week 4 of the intervention; through study completion, an average of 9 weeks
    Secondary Outcome Measure Information:
    Title
    Hair cortisol
    Description
    Objective stress markers will be measured via hair cortisol
    Time Frame
    Baseline; through study completion, an average of 9 weeks
    Title
    Serum adrenocorticotropic hormone (ACTH)
    Description
    Objective stress markers will be measured via serum ACTH.
    Time Frame
    Baseline; through study completion, an average of 9 weeks
    Title
    Serum cortisol
    Description
    Objective stress markers will be measured via serum cortisol.
    Time Frame
    Baseline; through study completion, an average of 9 weeks
    Title
    Serum norepinephrine
    Description
    Objective stress markers will be measured via serum norepinephrine
    Time Frame
    Baseline; through study completion, an average of 9 weeks
    Title
    Perceived Stress Scale.
    Description
    The Perceived Stress Scale queries participants' perceptions of feeling stress during the last month. Responses were on a 5-point scale from "never" to "very often." Scores will be summed to indicate current stress levels, with higher scores suggesting greater perceived stress (≥ 14 indicates moderate to high perceived stress).
    Time Frame
    Screening; through study completion, an average of 9 weeks
    Title
    Body fat mass
    Description
    Body fat mass will be measured via whole body dual energy x-ray absorptiometry (DEXA) scan.
    Time Frame
    Baseline; through study completion, an average of 9 weeks
    Title
    Body lean mass
    Description
    Body lean mass will be measured via whole body dual energy x-ray absorptiometry (DEXA) scan.
    Time Frame
    Baseline; through study completion, an average of 9 weeks
    Title
    Body bone density
    Description
    Body bone density will be measured via whole body dual energy x-ray absorptiometry (DEXA) scan.
    Time Frame
    Baseline; through study completion, an average of 9 weeks
    Title
    Triglycerides
    Description
    Will be measured from plasma by a commercial lab.
    Time Frame
    Baseline; through study completion, an average of 9 weeks
    Title
    High sensitivity C-reactive protein.
    Description
    Will be measured from plasma by a commercial lab.
    Time Frame
    Baseline; through study completion, an average of 9 weeks
    Title
    homeostasis model assessment-insulin resistance (HOMA-IR)
    Description
    calculated from fasting glucose and insulin using a standard formula.
    Time Frame
    Baseline; through study completion, an average of 9 weeks
    Title
    Microbial Deoxyribonucleic acid (DNA) isolation: 16S on V4 region
    Description
    performed on stool using Microbial DNA isolation
    Time Frame
    Baseline; through study completion, an average of 9 weeks

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    39 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: 18-39 years old. BMI 30-49.99 kg/m2. Own and use a smartphone, computer, or tablet with access to the Internet. Score ≥ 14 on the Perceived Stress Score (PSS) at screening. Exclusion Criteria: Have a personal or family history of EOCRC. Have taken antibiotics in the previous 2 months. Have an inflammatory bowel disease or genetic predisposition to EOCRC or CRC (e.g., Lynch syndrome);. Any cancer diagnosis or cancer treatment in the past 12 months. Consume >50 grams ethanol daily (approximately 4-5, 12 ounces beers). Use combustible tobacco. Have history of bariatric surgery or bowel resection. Have an active infection. Have type 1 or type 2 diabetes, immunodeficiency/autoimmune disorder, or inflammatory bowel disease. Use fiber or pre-/probiotic supplements >3 days per week. Currently taking corticosteroids medication - inhaled, topical, or oral in the past 2 months (affects cortisol measures). Are on a weight-loss diet or involved in a formal weight-loss program or are not weight stable for 3 months (+/- 4.5 kg) prior to the study. Females who are pregnant/trying to become pregnant. Have schizophrenia (medication can affect study outcomes). Have an eating window of <10 hours/day or are currently following an intermittent fasting pattern. Night shift workers (shift passes midnight). Present a history of eating disorder. Currently taking weight loss medication. Illegal drug use in the past month (not marijuana).
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Manoela Lima Oliveira, MS, RD, LDN
    Phone
    6189775345
    Email
    mlimao2@uic.edu
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Manoela Lima Oliveira, MS, RD, LDN
    Organizational Affiliation
    PhD Candidate
    Official's Role
    Principal Investigator
    First Name & Middle Initial & Last Name & Degree
    Lisa M Tussing-Humphreys, PHD, RD
    Organizational Affiliation
    Associate Professor, Kinesiology and Nutrition
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No
    Citations:
    PubMed Identifier
    35443109
    Citation
    Sinicrope FA. Increasing Incidence of Early-Onset Colorectal Cancer. N Engl J Med. 2022 Apr 21;386(16):1547-1558. doi: 10.1056/NEJMra2200869. No abstract available.
    Results Reference
    background
    PubMed Identifier
    22952311
    Citation
    Doubeni CA, Major JM, Laiyemo AO, Schootman M, Zauber AG, Hollenbeck AR, Sinha R, Allison J. Contribution of behavioral risk factors and obesity to socioeconomic differences in colorectal cancer incidence. J Natl Cancer Inst. 2012 Sep 19;104(18):1353-62. doi: 10.1093/jnci/djs346. Epub 2012 Sep 5.
    Results Reference
    background
    Links:
    URL
    https://redcap.link/mbsrandtre
    Description
    If you are interested in this research, please answer some eligibility questions in the survey linked here.

    Learn more about this trial

    Time-Restricted Eating and Mindfulness-Based Stress Reduction to Reduce the Risk of Early-Onset Colorectal Cancer

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