Trial · NCT02793531
Registered outcomes18
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
1 to 18 of 18
Download this page as JSON| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Change in net whole-body protein synthesis | 0, 2, 5, 10, 15, 20, 30, 40, 50, 60, 90, 120, 150, 180, 210, 225, 240, 260, 280, 300, 320, 340, 360 ± 5 min | Change in whole-body protein synthesis rate after intake of meal |
| Secondary | Body Composition | 15 minutes on screening or study day 1 | Body composition as measured by Dual-Energy X-ray Absorptiometry |
| Secondary | Skeletal muscle strength | on study day 1 | handgrip |
| Secondary | Skeletal muscle strength | on study day 1 | kin-com 1-leg test |
| Secondary | Respiratory muscle strength | on study day 1 | Maximum inhalation and exhalation pressure |
| Secondary | Gut function | In postabsorptive and prandial state every 20 minutes up to 6 hours before each sip feeding on study day | Digestion of the stable tracers of amino acid |
| Secondary | Group differences in state of mood as measured by the Hospital Anxiety and Depression Scale (HADS) | Postabsorptive state during 3 hours and change after feeding on study day 1 | a fourteen item self-assessment scale. Seven of the items related to anxiety and seven relate to depression. Each item on the questionnaire is scored from 0-3 and this means that a person can score between 0 (no symptoms) and 21 (severe symptoms) for either anxiety or depression. |
| Secondary | Group differences in activity as measured by Physical Activity Scale for the Elderly (PASE) | Postabsorptive state during 3 hours and change after feeding on study day 1 | questionnaire is intended for use in an elderly population and focuses on 3 types of activities: leisure time activities, household activities and work-related activities. |
| Secondary | Group differences in state of mood as measured by the Profile of Mood State (POMS) | Postabsorptive state during 3 hours and change after feeding on study day 1 | A psychological distress scale to measure mood disturbance in 6 domains - fatigue-inertia, vigor-activity, tension-anxiety, depression-dejection, anger-hostility, and confusion-bewilderment. Healthy populations take 3 to 7 minutes to complete, and others may take up a bit longer. |
| Secondary | appetite questionnaire | study day 1 | The subject is asked to rate various aspects of their appetite as relates to overall health |
| Secondary | Group differences in attention and executive functions as measured by Stroop Color-Word Test (SCWT) | Postabsorptive state during 3 hours and change after feeding on study day 1] | a word page with words printed in black ink, a color page with blocks printed in color, and a color-word page where the color and the word do not match. The examinee reads the words or names the ink colors as quickly as possible within a time limit. Measures selective attention and inhibitory control. The total time in seconds was reported for each trial. |
| Secondary | Group differences in learning and memory as measured by Controlled Oral Word Association Test (COWAT) | Postabsorptive state during 3 hours and change after feeding on study day 1 | The examinee is required to say as many words as they can think of in one minute that begin with a given letter of the alphabet. The task contains three trials. Measures phonetic verbal fluency. The raw score (total and mean words recorded across the three trials) was reported. |
| Secondary | Group differences in overall cognitive abilities as measured by Montreal Cognitive Assessment (MoCA) | Postabsorptive state during 3 hours and change after feeding on study day 1 | assesses several cognitive domains and is used for the screening of mild cognitive impairment. Total scores range from 0-30 with lower scores indicating decreased functioning. |
| Secondary | Group differences in attention and executive functions as measured by Brief-A | Postabsorptive state during 3 hours and change after feeding on study day 1 | a standardized self-report that captures views of an adult's executive functions or self-regulation in his or her everyday environment. |
| Secondary | diet recall | Postabsorptive state during 3 hours and change after feeding on study day 1 | The subject is asked to recall in detail all the food and drink consumed during the 24 hours prior to the test day. |
| Secondary | Group differences in attention and executive functions as measured by Trail Making Test (TMT) | Postabsorptive state during 3 hours and change after feeding on study day 1 | Part A, the examinee is instructed to connect a set of 25 circles with numbers as quickly as possible while maintaining accuracy. In Part B, the examinee is instructed to connect a set of 25 circles, alternating between numbers and letters, as quickly as possible while maintaining accuracy. Measures attentional resources and is a measure of the frontal lobe "executive" functions of visual search, set-switching and mental flexibility. The total time in seconds was reported for each measure. |
| Secondary | Functional Status | Postabsorptive state during 3 hours and change after feeding on study day 1 | Functional status will be assessed by the Karnofsky Performance Score, a widely used method to assess the functional status of a cancer patient. It describes a patient's functional status as a comprehensive 11-point scale ranging from 0% to 100%. |
| Secondary | Group differences in learning and memory as measured by Auditory Verbal Learning Test (AVLT) | Postabsorptive state during 3 hours and change after feeding on study day 1 | a verbal episodic memory test that evaluates a wide diversity of functions: short-term auditory-verbal memory, rate of learning, retention and recognition of information. |
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.
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