Trial · NCT06982612
Registered outcomes16
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
1 to 16 of 16
Download this page as JSON| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Plasma glucose | 8hours | Measured using colorimetric assay from venous blood samples |
| Secondary | Plasma insulin | 8hours | Measured using ELISA from venous blood samples |
| Secondary | Plasma osmolality | 8hours | Measured using freezing point depression from venous blood samples |
| Secondary | Plasma volume change | 8hours | Determined from haemoglobin and haematocrit measures in blood samples |
| Secondary | Urine volume | 8hours | Determined from urine samples collected before and after exercise |
| Secondary | Body mass | 8hours | Determined from weighing participants before and after exercise |
| Secondary | Urine specific gravity/osmolality | 8hours | Determined from urine samples collected before and after exercise |
| Secondary | Rectal temperature | 8hours | Measured via rectal probe |
| Secondary | Blood pressure | 8hours | Measured via and automated sphygmomanometer |
| Secondary | Respiratory gas exchanges | 8hours | Measured via Douglas bag, gas content and volume |
| Secondary | Rate of perceived exertion | 8hours | using Borg scales (from 6 \[no effort\] to 20 \[maximal effort\]) |
| Secondary | Rate of thermal sensation | 8hours | using -10 \[cold\] to +10 \[hot\] scale. |
| Secondary | Feelings of thirst, urge to urinate, GI comfort, and stomach bloatedness | 8hours | using scales (0 = no feeling, 10 = extreme feeling) |
| Other | N-back task for working memory (cognitive function) | 8hours | The task will comprise three progressively harder memory loads (1-Back, 2-Back, 3-Back). Each stimulus type will be used in all memory loads. Participants will have to respond using the space bar when they see a stimulus that is presented one, two, or three steps previously, dependent on the load condition. |
| Other | Go/no-go task for response inhibition (cognitive function) | 8hours | Participants will be instructed to press the space bar when a green image appears onscreen ("go" stimulus) and to inhibit responding when a red image is presented (the "no-go" stimulus). Increased commission error responses (i.e. responding incorrectly on a no-go trial) will indicate reduced response inhibition. Commission errors and correct responses will be measured as indices of performance. |
| Other | Stroop test | 8hours | The Stroop Test is a psychological assessment that measures a person's ability to inhibit cognitive interference and control attention. Typically, it involves naming the color of the ink in which a word is printed, even when the word itself names a different color (e.g., the word "red" printed in blue ink). The delay in response time when the word and ink color do not match-known as the Stroop effect-reflects the difficulty of suppressing automatic cognitive processes. |
Source ClinicalTrials.govtrials-2026-11-12-0.5.0
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this list from software.
Twenty rows a page, as JSON. No key.
GET https://conductscience.org/api/trials/v1/NCT06982612/registered