Evaluation of New Method for Measuring Stool Consistency

Evaluation of a New Method for Measuring Stool Consistency, Using a Texture Analyser (TA.XT Express Texture Analyser)

This study is designed to validate a new direct method for the measurement of stool consistency, using Texture Analyser. Forty healthy subjects are enrolled in this trial for collection of stool samples. Every stool produced during 2 collection periods of approximately 60 hours each is collected and subjected to the measurement of consistency using Texture Analyser. The stool consistency results are compared with the Bristol Stool Form Scale scores for each stool. The relationships of stool consistency with other stool parameters, bowel habit and sleeping habit are also evaluated.

Study Overview

• Status: Completed
• Conditions: Healthy
• Intervention / Treatment: Other: Collection of stool samples

Detailed Description

It is now obvious that the proper functioning of the gastrointestinal tract has a positive effect on the quality of life. Normal bowel habits vary considerably from person to person with regard to frequency of bowel movements, and bulk and consistency of stools. Constipation is the common digestive complaint in European populations, and softening stool consistency can be regarded as beneficial for such population in terms of reducing incidence of hard or lumpy stools .

The Bristol Stool Form Scale (BS) is validated as a surrogate measure for gastrointestinal transit time, and has been also applied to an evaluation of stool consistency. Subjects compare their stool with the BS chart consisting of seven categories and choose one score which has a nearest analog form. The BS has been widely used in the studies to evaluate changes in stool consistency after dietary intervention using probiotics and/or prebiotics. However, there is a lack of evidence in the validity of BS to yield consistent and reproducible estimates of changes in stool consistency over time. In order to obtain a closer estimate of its change, it would be preferred to use a more directly observable and objective parameter or combination of parameters.

From the above mentioned backgrounds, this study is conducted to validate a new direct method for the measurement of stool consistency, using Texture Analyser: TA.XTExpress Texture Analyser (Stable Micro Systems Ltd.).

• Study Type: Interventional
• Enrollment (Actual): 40
• Phase: Not Applicable

Contacts and Locations

Study Locations

• Belgium
  • Aalst, Belgium, 9300
    • Onze-Lieve-Vrouw Hospital Aalst

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (ADULT, OLDER_ADULT)
• Accepts Healthy Volunteers: Yes
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• Informed consent obtained before any study-related activities.
• Healthy female or male aged 18 years (inclusive) or older.
• Is willing and able to provide at least 3 stool samples during 2 collection periods of approximately 60 hours, to store the samples in appropriate conditions and to return the samples within the required timeframe.
• Is willing and able to complete a diary during the stool collection periods in order to collect information about form of the stools (based on the Bristol Stool Form Scale classification), bowel habit and sleep habit.
• Understands the Dutch or English language (reading, writing, speaking).

Exclusion Criteria:

• Language barrier, mental or legal incapacity, unwillingness or inability to understand or not being able to participate in this trial.
• Is treated (i.e., currently treated, treated within 1 month before inclusion) for constipation, diarrhoea or any other illness, by use of antibiotics or any other treatment with impact on defecation.
• Females of child bearing potential who are pregnant, breast-feeding or intend to become pregnant.
• Is unable to refrain from or anticipates the use of disallowed medications, e.g., antibiotics, laxatives, anti-diarrheal medication.
• Has any history of drug and/or alcohol abuse.
• Any clinically significant disease which in the Investigator's opinion could interfere with the safety of study participants or with the results of the study.
• Participation in another interventional clinical study or receipt of any investigational product within 1 month before visit 1.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: OTHER
• Allocation: NA
• Interventional Model: SINGLE_GROUP
• Masking: NONE

Number of Arms

1

Arms and Interventions

Participant Group / Arm

Intervention / Treatment

OTHER: Specimen collection; Collection of stool samples

Other: Collection of stool samples; The subjects collect stool samples to be used for validation of a new direct measurement of stool consistency. Every stool sample produced during 2 collection periods of approximately 60 hours each have to be collected using the Commode Specimen Collection System (Medline Industries, Inc.). Each collection period starts preferably in the evening (20h00) and ends 3 days later in the morning (08h00). The collected samples must be stored at subject's home in a refrigerator provided by the sponsor until handover to the site staff.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Stool consistency	Stool consistency is measured as force (g) during compression by Texture Analyser. A cylinder probe is put vertically into the object with a constant speed and the force is measured when reaching down to the target (5 mm down from the surface) as an outcome.	Two stool collection periods of approximately 60 hours each

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Bristol Stool Form Scale score	Bristol Stool Form Scale (BS) is for classifying the form of stool into 7 categories scored from 1 to 7; (1) Separate hard lumps like nuts (difficult to pass); (2) Sausage-shaped but lumpy; (3) Like a sausage but with cracks on its surface; (4) Like a sausage or snake, smooth and soft; (5) Soft blobs with clear-cut edges (passed easily); (6) Fluffy pieces with ragged edges, a mushy stool; (7) Watery, no solid pieces, entirely liquid. Subjects choose one of the BS scores which has a nearest analog form with their stools at every defecation.	Two stool collection periods of approximately 60 hours each
Stool water content	Percentage of water in stool (weight/weight %)	Two stool collection periods of approximately 60 hours each
Stool mucin	Concentration of mucin in stool	Two stool collection periods of approximately 60 hours each
Stool pH	Degree of stool pH	Two stool collection periods of approximately 60 hours each
Stool metabolites	Concentrations of stool metabolites including organic acids	Two stool collection periods of approximately 60 hours each
Stool microbiota composition	Relative abundance of microbiota species (% of total) in stool	Two stool collection periods of approximately 60 hours each
Stool amount	Weight (g) of stool produced in each defecation	Two stool collection periods of approximately 60 hours each
Bowel habit	Presence or absence of straining during evacuation, presence or absence of sensation of remaining stool in the rectum after evacuation	Two stool collection periods of approximately 60 hours each
Sleep habit	Getting-up time, going-to-bed time and sleeping hours	Two stool collection periods of approximately 60 hours each

Collaborators and Investigators

• Sponsor: Yakult Honsha European Research Center, ESV
• Collaborators: Harmony Clinical Research BVBA
• Investigators: Principal Investigator: Ignace Demeyer, Dr., Onze-Lieve-Vrouw Hospital Aalst

Study record dates

Study Major Dates

• Study Start (ACTUAL): June 2, 2017
• Primary Completion (ACTUAL): July 6, 2017
• Study Completion (ACTUAL): July 6, 2017

Study Registration Dates

• First Submitted: June 8, 2017
• First Submitted That Met QC Criteria: June 14, 2017
• First Posted (ACTUAL): June 15, 2017

Study Record Updates

• Last Update Posted (ACTUAL): November 9, 2017
• Last Update Submitted That Met QC Criteria: November 7, 2017
• Last Verified: November 1, 2017

More Information

Terms related to this study

• Keywords: Bristol Stool Form Scale; Stool consistency; Texture Analyser
• Other Study ID Numbers: YHER16-TAXT

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No