The Acute Effects of Low Temperature for Long Time Heat Treatment of Pork Semitendinosus on Satiety (SAPO)

May 3, 2017 updated by: Anne Birgitte Raben, University of Copenhagen

Cooking meat at low temperatures for prolonged times is widely used among chefs and in food service due to the possibility to obtain a consistent and appealing eating quality. The method is generally termed low-temperature long-time (LTLT) cooking. In LTLT cooking, meat is vacuum-packed and heated at temperatures between 50°C and 65°C in a water bath for several hours. LTLT has several benefits - improved tenderness and juiciness, less cooking loss, better vitamin retention and uncompromised food safety.

A recent PhD thesis concluded that one of the mechanisms behind the changes in eating quality during LTLT cooking was due to the proteolytic degradation in the muscle tissue. The activity of proteolytic enzymes has shown to be dependent on heating temperature and time where the cathepsins were found to remain active during heat treatment. At 58°C the cathepsin B+L activity is increased compared to 48°C and 53°C and at 55°C compared to 25°C, 40°C and 70°C. A prolonged heating time of 17 hours at 58°C has also shown to increase cathepsin B+L activity. The proteolytic degradation results in the occurrence of peptides and amino acids such as tryptophan, tyrosine, leucine and histidine which could lead to a faster degree of satiety when consumed.

According to the aminostatic hypothesis by Mellinkoff, a rise in plasma amino acids elicited by protein ingestion could assist in the suppression of food intake and the onset of satiety.

The investigators therefore hypothesize that the ingestion of LTLT cooked pork would induce a faster satiety response due to the higher availability of peptides and amino acids prior to digestion. An acute meal study will elucidate this. LTLT cooking will be performed by the "cook-chill" method to mimic real life where meat is rapidly chilled after heat treatment, stored at 0-2°C and reheated and browned prior to serving.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

40

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Taastrup, Denmark, 2630
        • Danish Meat Research Institute

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 60 years (Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

Male

Description

Inclusion Criteria:

  • Participants who have provided written informed consent
  • Healthy men
  • Ages between 18 and 60 years
  • BMI between 18.5 and 30 kg/m2
  • Pork eaters

Exclusion Criteria:

  • Any food allergy, dislike or special diet of relevance to the study (e.g. vegetarian)
  • Daily use of prescription medicine or over-the-counter drugs affecting appetite, energy expenditure or protein metabolism
  • Use of dietary supplements (including protein supplement, powders, shakes) up to 1 month before the first meal test
  • Irregular eating schedule (e.g. skipping breakfast)
  • Self-reporting currently dieting or having lost/gained significant amount of weight (±3 kg) in the previous 3 months
  • Any known chronic diseases (e.g. cancer, heart disease, diabetes, neurological disorders)
  • Vigorous physical activity more than 10 hours/week
  • Smoking, smoking cessation within the past 3 months or nicotine use (electronic cigarettes) (>10 cigarettes per day)
  • Participants who work in appetite or feeding related areas
  • Participation in other intervention studies
  • Participants not able to comply with the study protocol as judged by study personnel

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Crossover Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Pork, 58°C, 72 minutes
Pork muscle (semitendinosus) sous-vide cooked at 58°C for 72 minutes
Experimental: Pork, 58°C, 17 hours
Pork muscle (semitendinosus) sous-vide cooked at 58°C for 17 hours
Experimental: Meat balls, 58°C, 17 hours
Meat balls made from pork Semitendinosus. Sous-vide cooked at 58°C for 17 hours
Active Comparator: Pork, 160°C (until 58°C in core)
Pork muscle (semitendinosus) oven cooked at 160°C until 58° in core.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Ad libitum energy intake
Time Frame: 180 min
the primary outcome is measured 180 min after test meal is consumed
180 min

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
VAS scores for appetite (hunger, satiety, fullness, prospective consumption)
Time Frame: every 30 min at time points 15, 45, 75, 105, 135, 165, 195 min from termination of the test meal.
The secondary endpoints are measured every 30 minute after the test meal is consumed
every 30 min at time points 15, 45, 75, 105, 135, 165, 195 min from termination of the test meal.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

November 1, 2014

Primary Completion (Actual)

December 1, 2014

Study Completion (Actual)

December 1, 2014

Study Registration Dates

First Submitted

November 10, 2014

First Submitted That Met QC Criteria

July 10, 2015

First Posted (Estimate)

July 13, 2015

Study Record Updates

Last Update Posted (Actual)

May 8, 2017

Last Update Submitted That Met QC Criteria

May 3, 2017

Last Verified

May 1, 2017

More Information

Terms related to this study

Other Study ID Numbers

  • SAPO 2A

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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