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Chickpea study: does hummus vs. pasta change how you burn energy?

NCT ID NCT06758869

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 2 times

Summary

This study looks at how eating chickpeas in different forms—whole, pureed (like hummus), or as flour (like pasta)—affects how the body uses energy. Researchers will measure fat, carbohydrate, and protein burning in 204 healthy adults over 12 weeks. The goal is to understand if processing changes the health benefits of pulses.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
chickpea-based food products (whole chickpeas, pureed chickpeas, chickpea flour pasta)
What this could lead to
If successful, this could show that how a food is processed changes how our bodies use it for energy, which may help design healthier diets.
What could go wrong
This is an early-stage observational study in healthy people, not a treatment trial. Results may not apply to people with health conditions, and the effects might be small or hard to measure.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 204 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Jan 2027

An estimate. Start dates often move.

Expected to finish

Dec 2029

An estimate. End dates often move.

Lead sponsor

A government agency

The lead sponsor is a US federal agency other than the NIH.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

19 to 60 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

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

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As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

How to take part

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  1. The places running it

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  2. The official record

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  3. A doctor treating you

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Contacts and locations

Locations

  • USDA Grand Forks Human Nutrition Research Center

    Grand Forks, North Dakota, 58203, United States

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