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Recruiting NCT07255183

Glucose and Motivation States

No phase Interventional Motivation

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Exercise, Sugar Drink, Non-sugar beverage.
Who it may be relevant to
Registry conditions: Motivation. Basic parameters: 18 years — 45 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

Impact of Blood Glucose on Motivation States: A Double-Blind Placebo-Controlled Study

Overview

The purpose of this study is to evaluate how motivation is impacted by exercise and beverage consumption. You will be asked to report to our lab for 5 visits each separated by 2+ days over a period of 2-3 weeks.

Interventions

  • Behavioral Exercise
    Exercise 30 minutes at moderate intensity (10% below ventilatory threshold)
  • Dietary supplement Sugar Drink
    Consume 250mL beverage (water + 6 tablespoons table sugar)
  • Dietary supplement Non-sugar beverage
    Consume 250mL beverage (water + 1.5 teaspoons of stevia powder)

Primary outcome measures

  • State Motivation to Move [Time frame: 60 minutes]
Secondary outcome measures (1)
  • State motivation to rest [Time frame: 60 minutes]

Eligibility criteria

Inclusion criteria

  • Body mass index 18-30 m/kg\^2
  • Health Status: generally healthy; no cardiopulmonary/metabolic/orthopedic disease or limitations
  • Blood Pressure: excluded with SBP of 130+ mmHg or DBP of 80+ mmHg
  • Glucose Status: excluded and instructed to seek medical consultation if fasting values are <70 mg/dl or >125 mg/dl; included but encouraged to seek medical consultation if fasting values are 100-125 mg/dl

Exclusion criteria

  • None

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Crossover
Masking
Triple blind
Primary purpose
Basic science

Study locations

United States · 1 center
  • University of South Florida — Tampa

Identifiers

NCT: NCT07255183 · STUDY009043

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗