- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03282708
Comparative Study of Great Ape-caretaker Microbiome (SHAPES-CAP)
Comparative Study of Captive Great Ape and Human Intestinal Microbiomes
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Paris, France, 75724
- Institut Pasteur
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
For both Microbiome and Anthropology sub-study
- Adult in good health
- Currently working as a caretakers of captive great apes
For Microbiome sub-study
- Agree to autonomous collection of a stool sample
- Agree to return the stool specimen inside of a designated, supplied postal container and box.
For Anthropology sub-study:
- Accept to be observed during his or her professional activity two times, each time for a duration of four hours by the researchers
Exclusion Criteria:
For both Microbiome and Anthropology parts:
- Protected adults, pregnant and nursing mothers will not be included.
For Microbiome sub-study
- Patients, especially those with gastrointestinal disorders (diarrhea), frequent and/or liquid stools, abdominal pain, nausea, vomiting, fever
- Anyone diagnosed with a chronic disease
- Anyone who has taken an antibiotic or antifungal treatment in the month preceding collection.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Microbiome
Caretakers of captive great apes. One sample collection of spontaneously produced fresh stool (of an approximate size of 3 green beans). Data collection with self-administered questionnaire |
One sample collection of spontaneously produced fresh stool (of an approximate size of 3 green beans). Data collection with self-administered questionnaire |
|
No Intervention: Anthropology
Caretakers of captive great apes.
Two four-hour participant-observations of each caretaker's activities with captive great apes
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Microbiome comparison
Time Frame: Three years (September 2017-September 2020)
|
The investigators will evaluate the components of the intestinal microbiome (viral and bacterial enterotypes) shared by human caretakers and captive great apes living in proximity on a daily basis.
The percentage of overlap (of viral and bacterial families) between human subjects and great apes will be measured.
|
Three years (September 2017-September 2020)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Contact type investigation
Time Frame: Three years (September 2017-September 2020)
|
The investigators will evaluate the type of physical contact between caretakers and great apes in captivity through participant-observations.
This outcome will be measured through identified categories of physical contact.
|
Three years (September 2017-September 2020)
|
|
Contact frequency investigation
Time Frame: Three years (September 2017-September 2020)
|
The investigators will evaluate the frequency of physical contact between caretakers and great apes in captivity through participant-observations.
This outcome will be measured by the number per category of physical contact.
|
Three years (September 2017-September 2020)
|
|
Contact duration investigation
Time Frame: Three years (September 2017-September 2020)
|
The investigators will evaluate the duration of physical contact between caretakers and great apes in captivity through participant-observations.
This outcome will be measured by the duration (time) per individual contact.
|
Three years (September 2017-September 2020)
|
Collaborators and Investigators
Sponsor
Investigators
- Study Director: Tamara Giles-Vernick, PhD, Institut Pasteur
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 2016-081
- ID-RCB: 2017-A00734-49 (Other Identifier: French national registration number of the study)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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