- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05534152
Effect of Sumac on Appetite and Food Intake
The Effect of Consumption of Sumac in Vegetable Soup on Appetite and Food Intake Among Older Adults (Aged Over 65 Years) and Young Adults (Aged 18-35 Years)
Study Overview
Detailed Description
Rhus coriaria Linn, also known as Sumac, is a spice that is widely used in Turkish, Iranian and Middle Eastern foods. In these regions, the fruit of sumac is used for seasoning or flavouring, as an appetizer and for souring food. This spice has also been used in herbal folk medicine to relieve certain conditions including bowel disorders, anorexia and indigestion. In addition, many studies have shown that sumac contains a high level of antioxidant activity and polyphenol content that may benefit certain diseases such as cancer and diabetes.
Taste and smell perception may play a vital role in food preference, nutrient intake and appetite; however, both ageing and disease can have a negative impact on these senses. It has been suggested that by 2025 the older adult population (i.e. those aged 60years and over) worldwide will rapidly increase and reach 1.12 billion. One of the major physiological changes in this age group is the loss or reduction in sensory perception including smell and taste. These changes as a result of ageing and medication increase the risk of poor health by reducing the enjoyment of food followed by decreasing food and nutrient intake.
It is possible, therefore, that all these factors together may lessen the enjoyment of food, leading to malnutrition and disease complications. In light of the above, the aim of this study was to assess the level of the appetite and food intake among young adults in comparison with free living older adults following the consumption of sumac. This was achieved by assessing the amount of food intake during a lunch course and the impact on food intake for the subsequent 12 hours.
This study assessed the use of sumac at 1% dose (0.37g) of total volume of a vegetable soup (150g), in two forms: 1) added to finished cooked soup 2) added to the soup from the beginning of the cooking process, in addition to consumption of the same soup without added sumac as the control soup. The study comprised of 20 young adults (18-35 years old) and 20 free living older adults aged >65 years. Each participant in these groups attended the Oxford Brookes Centre for Nutrition and Health (OxBCNH) for three sessions and each session lasted up to one hour.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Oxford, United Kingdom, OX3 0BP
- Oxford Brookes Centre for Nutrition and Health
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
• Adults, aged >65 years
- Adults, 18-35 years
- No allergy to any herbs and spices
- No allergy to vegetables including celery and tomato
- Non-smoker
- Do not have a cold or hay fever (on test day)
- No medication that may affect the sensory taste such as: antibiotics, antihistamines and decongestants, anti-inflammatory agents, and muscle relaxants (Bromley, 2000)
- Ability to read and understand written information in English
- Ability to attend, stand and sit for up to one hour
- The normal level of capability of functional activity (i.e. traveling out to the neighbourhood, shopping alone)
- Not diagnosed with Dementia
Exclusion Criteria:
- Disease that may affect the taste and smell sensation including local chronic or acute inflammatory nasal disease and oral and perioral infections
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Placebo Comparator: Soup with no sumac
150 g butternut squash soup with no added sumac
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1% iranian brown sumac
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Experimental: Sumac added to soup at the end of cooking
150 g butternut squash soup with 1% sumac added at the end of cooking
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1% iranian brown sumac
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Experimental: Sumac added to the sumac during cooking
150 g butternut squash soup with 1% sumac added during cooking
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1% iranian brown sumac
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Energy intake in kilojoules and kilocalories
Time Frame: 9 hours
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Energy intake at an ad libitum lunch after the soup and for the rest of the day using Nutritics dietary assessment software.
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9 hours
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Carbohydrate intake in grams
Time Frame: 9 hours
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Carbohydrate intake at an ad libitum lunch after the soup and for the rest of the day using Nutritics dietary assessment software.
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9 hours
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Protein intake in grams
Time Frame: 9 hours
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Protein intake at an ad libitum lunch after the soup and for the rest of the day using Nutritics dietary assessment software.
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9 hours
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Fat intake in grams
Time Frame: 9 hours
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Fat intake at an ad libitum lunch after the soup and for the rest of the day using Nutritics dietary assessment software.
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9 hours
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Amount of food consumed at lunch in grams
Time Frame: 9 hours
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Amount of food (pasta) consumed in grams at the ad libitum lunch
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9 hours
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Sangeetha Thondre, PhD, Oxford Brookes University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- UREC 181174
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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