Farms, Animals and Adolescents: Reinforcing the Microbiome

NCT ID: NCT03189849

Last Updated: 2017-10-26

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 11 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2017-05-10
• Study Completion Date: 2017-09-30

Brief Summary

This study will be an observational study of children who attend summer camp at the Heartland Farm Sanctuary (HFS). The investigators are exploring whether time-limited exposure to a traditional farming environment will improve children's overall health and general well-being.

Detailed Description

The overarching hypothesis for this study is that urban children exposed on a time-limited basis to a traditional farming environment will show increased beneficial bacteria in the gut microbiome and enhanced emotional well-being. Secondary hypotheses are that 1) increased presence of farm-derived immunoregulatory micro-organisms in the nose (indicating exposure) will be associated with measures of emotional well-being and prosocial behavior. To test these hypotheses, 40 urban children ages 7-13 years will be studied prior to and following a 1, 2, or 3-week camp experience at the Heartland Farm Sanctuary summer camp program in Verona, WI. Assessments for behavior (via questionnaires), gut microbiota composition and function (via stool) and presence in the body of farm-derived immunoregulatory micro-organisms (via nasal swab) will be assessed at baseline (2 weeks before the start of camp and the weekend before camp starts), immediately following the child's 1, 2, or 3-week camp experience and at 1 month following completion of the camp experience. Importantly, this assessment schedule will allow the investigators to assess the longevity of any observed physical or behavioral changes induced by exposure to the farming environment.

Conditions

Healthy

Keywords

Farming environment

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Eligibility Criteria

Inclusion Criteria

• Males and females ages 7-13 years
• Able to attend camp at Heartland Farm Sanctuary for either 1, 2, or 3 consecutive weeks (if not consecutive, but within a 4-week period, this is allowable)
• In generally good health
• Have not taken antibiotics in the four weeks prior to when their first baseline set of samples will be collected
• Have not attended camp at HFS or regular volunteer activities at HFS in the past year (participation in previous summer HFS camp is permissible)
• Able to understand the nature of the study and able to provide assent
• Able to communicate in English with study personnel.
• Willing to commit to participating in the study and doing the home collection of samples.

• Parent or legal guardian of a child attending HFS summer camp and participating in this study
• Willing to assist the child in the collection of samples as necessary
• Willing to answer questionnaire about their child's participation in the study
• Able to communicate in English with study personnel

Exclusion Criteria

• Individuals who will not be able to collect the samples for any reason, including planned vacations, unwillingness, or inability. (Note - children who are attending either 2 or 3 weeks of camp and who take a break in between weeks of camp will be allowed to participate if their full two or three-week camp exposure occurs within a 4-week period).
• Plan to attend camp during the fall (i.e. during their month 1 month follow-up)
• Children living in farming environments prior to camp participation
• Children with more than an average of one exposure per week to farm animals, livestock, horses
• Individuals currently on any antibiotic therapy or who will require chronic and/or periodic antibiotic treatment during the study period.
• Subject has a medical condition or disorder that

• Is unstable, or:
• Could interfere with the accurate assessment of safety or efficacy of the clinical assessments, including individuals with any:
• Current participation in any clinical trial that might impact results of this one, which includes participation in another clinical trial where any experimental drugs are being taken as well as studies / drug trials with agents that might affect mood and or the gastrointestinal tract.
• Reasonable likelihood for non-compliance with the protocol for any other reason, in the opinion of the Investigator, prohibits enrollment of subject into the study.

• Unwilling to assist their child in collection of the samples for this study
• Unwilling to answer questionnaire about their child's participation in the study
• Unable to communicate in English with study personnel

• Minimum Eligible Age: 7 Years
• Maximum Eligible Age: 13 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

University of Wisconsin, Madison

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

University of Wisconsin-Madison

Madison, Wisconsin, United States

Countries

United States

Other Identifiers

2017-0154

Identifier Type: -

Identifier Source: org_study_id