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Pulse Revolution: Enhancing Metabolic Health Through the Power of Processed Chickpeas

U

USDA Grand Forks Human Nutrition Research Center

Status

Not yet enrolling

Conditions

Healthy

Treatments

Other: Whole Chickpeas
Other: Control
Other: 100% Chickpea Flour Product
Other: Puréed Chickpeas

Study type

Interventional

Funder types

Other U.S. Federal agency

Identifiers

NCT06758869
GFHNRC514

Details and patient eligibility

About

The purpose of this research is to test how processing can affect how one's body uses the nutrients in that food. For this study the researchers are examining how making different food products out of chickpeas, such as hummus or pasta, changes how one's body uses those foods for energy.

Full description

The overall objective is to determine the impact of daily consumption of processed pulse-based food products on metabolic health, specifically the physiological responses related to energy metabolism. The primary hypothesis is that consuming a serving of pulses daily for 12 weeks will improve metabolic responses related to energy metabolism, particularly fat oxidation and molecular adaptations related to fat and glucose metabolism, compared to current Dietary Guidelines for Americans (DGA) recommendations. Furthermore, we hypothesize that the degree of processing will influence these metabolic adaptations such that the daily consumption of 100% pulse flour food products will result in the greatest effect on fat oxidation and molecular adaptations related to fat and glucose metabolism followed by the pulse purée which will have a greater effect than the whole cooked pulse (100% pulse flour > purée > whole).

Enrollment

204 estimated patients

Sex

All

Ages

19 to 60 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • apparently healthy adults
  • BMI >18.5 or <35 kg/m2 (healthy body weight - class I obesity)
  • ability to understand and sign the consent form
  • availability of transportation (i.e., participants must provide their own transportation to the Center)
  • non-smoking or do not use other tobacco products, including e-cigarettes
  • not taking steroid-based medications
  • not planning to or currently attempting to gain or lose weight
  • not allergic to study foods
  • willing to comply with study demands

Exclusion criteria

  • usual pulse consumption greater than DGA recommendation
  • inability or unwillingness to consume any of the provided foods
  • more than a 10% change in body weight within the past 2 months
  • actively trying to lose weight
  • pregnancy or actively trying to get pregnant
  • lactation
  • uncontrolled hypertension (systolic >160 mmHg or diastolic >100 mmHg)
  • diagnosed cardiovascular, pulmonary, skeletal and metabolic diseases
  • HbA1c ≥ 5.7%
  • complete blood count (CBC) outside of the normal range for a healthy adult
  • history of gastrointestinal (GI) disorders (including Celiac's or Crohn's disease, irritable bowel syndrome, acid reflux, ulcerative colitis, chronic constipation or diarrhea, and lactose intolerance)
  • using medications known to affect appetite, blood lipids, body composition, body weight, or food intake (appetite control drugs, steroids)
  • cannot read or understand English

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

204 participants in 4 patient groups

Control
Experimental group
Description:
Base DGA diet with a standardized non-pulse product snack
Treatment:
Other: Control
Whole Chickpeas
Experimental group
Description:
Adjusted DGA diet with standardized whole chickpea snack
Treatment:
Other: Whole Chickpeas
Puréed Chickpeas
Experimental group
Description:
Adjusted DGA diet with standardized puréed chickpea snack
Treatment:
Other: Puréed Chickpeas
100% Chickpea Flour Product
Experimental group
Description:
Adjusted DGA diet with standardized 100% chickpea flour product snack
Treatment:
Other: 100% Chickpea Flour Product

Trial contacts and locations

1

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Central trial contact

Shanon Casperson, PhD

Data sourced from clinicaltrials.gov

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