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Efficacy of Pea Hull Fiber - Phase 2

Efficacy of Pea Hull Fiber Supplementation on Gastrointestinal Transit in Overweight Children.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03016065
Enrollment
18
Registered
2017-01-10
Start date
2017-03-29
Completion date
2022-11-15
Last updated
2022-11-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy

Brief summary

The purpose of this randomized, cross-over study is to explore the effects of pea hull fiber on bowel movement frequency, transit time, appetite, gastrointestinal symptoms, microbiota composition and activity.

Detailed description

An 8-week randomized, cross-over study will be carried out to assess the efficacy of pea hull fiber. Participants will complete a 2-week baseline period during which appetite, stool frequency, and stool consistency (transit time) will be collected by an online questionnaire, and participants will collect a single stool. Dietary data (Automated Self-Administered 24-Hour diet recall) will be obtained at baseline and at each study visit. Participants will be randomized on or about day 15 and consume snacks without pea hull fiber for a 2-week control period, and snacks with added pea hull fiber for a 2-week treatment period separated by a 2-week washout period. In both intervention periods, participants will complete daily questionnaires to assess stool frequency and consistency (transit time). An online questionnaire assessing appetite will be administered once per week. The GSRS will be competed at each study visit. During washout periods, the same data will be collected as will be done during the baseline and intervention periods. Participants will be asked to collect one stool during baseline and during weeks 4, 6, and 8 for a total of 4 stools. Stool samples will be analyzed for changes in the microbiota.

Interventions

DIETARY_SUPPLEMENTPea Fiber

Baked goods (2 snacks) with fiber-fortified with 5 g/snack of ground pea hulls

DIETARY_SUPPLEMENTControl

Baked goods (2 snacks) without added fiber

Sponsors

Saskatchewan Pulse Growers
CollaboratorOTHER
University of Florida
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
8 Years to 15 Years
Healthy volunteers
Yes

Inclusion criteria

* Are willing to have height and weight measured and provide demographic information (e.g. age, race, sex). * Children age between 8-15 years old. * Are occasionally constipated. * Are willing to consume pea hull fiber and control snacks daily each for a 2-week period * Are willing to complete a daily questionnaire throughout the entire 8-week study. * Are willing to complete the appetite questionnaire two times per week. * Are willing to complete the Gastrointestinal Symptom Rating Scale (GSRS) bi-weekly. * Are willing to be interviewed for Automated Self-Administered 24-Hour-Kids-2014 (ASA24-Kids-2014) one time per 2-week period throughout the study. * Are willing and be able to provide a valid social security for study payment purposes.

Exclusion criteria

* Have any known food allergies. * Are currently taking medications for diarrhea. * Have taken antibiotics within the past four weeks prior to randomization. * Have ≥ 6 bowel movements per week * Are currently taking probiotics supplements and do not want to discontinue a minimum of two weeks prior to the study. * Have previously or are currently being treated for any gastrointestinal diseases such as (gastric ulcers, Crohn's, Celiac, ulcerative colitis, etc.).

Design outcomes

Primary

MeasureTime frameDescription
Change in Modified Bristol Stool Form scoreChange from baseline at weeks 4, 6 and 8Stool consistency rating by Modified Bristol Stool Form for children

Secondary

MeasureTime frameDescription
Change in number of bowel movements per weekChange from baseline at weeks 4, 6 and 8Stool frequency per week

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026