Influence of Different Sugary Beverages on Thirst Sensation
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Purpose
The purpose of this study is to determine if water and three different sugary beverages (milk, Orange juice and iced tea) have the same effect on thirst.
| Condition | Intervention |
|---|---|
|
Thirst |
Behavioral: Effect of ingestion of different Sugary Beverages on Thirst Sensation |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Intervention Model: Crossover Assignment Masking: Single Blind (Subject) Primary Purpose: Diagnostic |
| Official Title: | Influence of Different Sugary Beverages on Thirst Sensation |
- Motivational Ratings [ Time Frame: 1 day ] [ Designated as safety issue: No ]
Participants will rate their hunger, thirst, nausea, mouth dryness, desire to eat, desire to drink using nine point category scales. The unipolar adjective scales were anchored at each end with labels: 1 = not at all and 9 = extremely.
Participants also rated their liking for the beverage along nine point hedonic preference scales where 1 = dislike extremely and 9 = like extremely.
- Glycaemia [ Time Frame: 1 day ] [ Designated as safety issue: Yes ]Glycaemia will be assessed before and after the ingestion of beverages
- Amount of water ingested [ Time Frame: 1 day ] [ Designated as safety issue: No ]After the ingestion of 3 preloads with the beverages in study, the participants will lunch the same meal with free water ingestion.
- Food Behavior After Intervention [ Time Frame: 1 day ] [ Designated as safety issue: No ]After lunch, participants will bring a food diary to record all food and fluid intake until 00.00 that day. Then, we will analyse total calories ingested, total fluid ingested and the volume of sugar and sugary beverages ingested.
- Blood osmolality [ Time Frame: 1 day ] [ Designated as safety issue: Yes ]Blood osmolality will be assessed before and after the ingestion of beverages
- Plasmatic Sodium [ Time Frame: 1 day ] [ Designated as safety issue: Yes ]Plasmatic sodium will be measured before and after the ingestion of the beverages.
- Hydration parameters [ Time Frame: 1 day ] [ Designated as safety issue: Yes ]Total body water, intra and extracellular body water will me measured before and after the ingestion of the beverages
| Enrollment: | 32 |
| Study Start Date: | June 2012 |
| Study Completion Date: | August 2012 |
| Primary Completion Date: | July 2012 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Placebo Comparator: Group 1 (placebo) - Water
This group will drink water in 1st trial
|
Behavioral: Effect of ingestion of different Sugary Beverages on Thirst Sensation
The participants will drink Water (control group),Non-fat Milk, Orange Juice and Iced Tea. The beverages will be presented chilled but without ice in 330 ml portions in opaque plastic containers and participants will be asked to consume the entire amount within 15 min.
|
|
Experimental: Group 2 (Intervention) - Milk
This group will drink Non-Fat Milk in 1st trial
|
Behavioral: Effect of ingestion of different Sugary Beverages on Thirst Sensation
The participants will drink Water (control group),Non-fat Milk, Orange Juice and Iced Tea. The beverages will be presented chilled but without ice in 330 ml portions in opaque plastic containers and participants will be asked to consume the entire amount within 15 min.
|
|
Experimental: Group 3 (Intervention) - Orange Juice
This group will drink Orange Juice in 1st trial
|
Behavioral: Effect of ingestion of different Sugary Beverages on Thirst Sensation
The participants will drink Water (control group),Non-fat Milk, Orange Juice and Iced Tea. The beverages will be presented chilled but without ice in 330 ml portions in opaque plastic containers and participants will be asked to consume the entire amount within 15 min.
|
|
Experimental: Group 4 (Intervention) - Iced Tea
This group will drink Iced Tea in 1st study
|
Behavioral: Effect of ingestion of different Sugary Beverages on Thirst Sensation
The participants will drink Water (control group),Non-fat Milk, Orange Juice and Iced Tea. The beverages will be presented chilled but without ice in 330 ml portions in opaque plastic containers and participants will be asked to consume the entire amount within 15 min.
|
Detailed Description:
Participants should be in the laboratory at 8.00 in order to collect the values of weight, height, total body water, intracellular water and extracellular water in a Segmental Multi Frequency Body Composition Monitor (TANITA MC 180 MA®). Then, a blood sample will be collected for analysis of blood glucose, osmolality and plasmatic sodium. They will sit at individual tables for the duration of the session and were allowed to read, listen to music with earphones, or use their portable computers with the exception of internet access to minimize visual cues (e.g., unwanted publicity for beverages or visiting Web sites showing pictures of food and drinks), which may have effect on thirst. Breakfast will be served at 9.30 on every occasion and preload stimuli will be offered exactly 60 minutes after breakfast (at 10.30). Lunch will be provided at 13.00. Motivational ratings will be first obtained at the end of collection of blood sample (baseline or time 0) and every 30 minutes thereafter until the lunch time (times 1 through 7). After lunch (time 8), participants will complete the last set of ratings and will bring a food diary to record all food and fluid intake until 00.00 that day.
Eligibility| Ages Eligible for Study: | 18 Years to 65 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
- body mass index(BMI) between (18,5 - 27,5 kg/m2)
- regular consumers of breakfast
- stable in weight for the past 6 months
- not dieting to gain or lose weight
- like all drinks and food available in study
Exclusion Criteria:
- pregnant and nursing women
- smokers
- athletes
- subjects under medication(except oral contraceptives in women)
Contacts and Locations| Portugal | |
| Faculty of Nutrition and Food Sciences - University of Porto | |
| Porto, Portugal, 4200-465 | |
| Principal Investigator: | Pedro R Carvalho, PhD Student | FCNAUP |
More Information
No publications provided
| Responsible Party: | Pedro Miguel Fernandes Ramos de Carvalho, Invited Assistant, Universidade do Porto |
| ClinicalTrials.gov Identifier: | NCT01770327 History of Changes |
| Other Study ID Numbers: | EHI-FCNAUP, Nº30/CEUP/2011_2 |
| Study First Received: | January 15, 2013 |
| Last Updated: | January 18, 2013 |
| Health Authority: | Portugal: Health Ethic Committee |
ClinicalTrials.gov processed this record on June 18, 2013