Trials / Recruiting
RecruitingNCT06672952
Dose-Response Impact of Glucosyl-Hesperidin (CitraPeak) on Exercise Performance, Blood Flow, Stress, Cognition, and Other Perceptual Indicators
- Status
- Recruiting
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 60 (estimated)
- Sponsor
- Lindenwood University · Academic / Other
- Sex
- All
- Age
- 18 Years – 50 Years
- Healthy volunteers
- Accepted
Summary
The purpose of this study is to evaluate the dose-dependent effects of glucosyl-hesperidin (CITRAPEAK) supplementation on exercise performance, recovery indicators, blood flow, cognitive function, mood, sleep, and fuel utilization in recreationally active adults.
Detailed description
This randomized, double-blind, placebo-controlled study investigates the effects of glucosyl-hesperidin (CITRAPEAK) on exercise performance, recovery, cognitive function, mood, and cardiovascular health in approximately 60 healthy, recreationally active adults aged 18-50. Participants will be assigned to one of three groups (placebo, 200mg CITRAPEAK, or 400mg CITRAPEAK) based on sex and baseline fat-free mass. Each participant will consume their assigned supplement daily for 8 weeks, with adherence tracked via supplementation logs. The study includes multiple visits, where participants will undergo a range of assessments, including exercise performance tests, blood flow analysis, and cognitive evaluations.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DIETARY_SUPPLEMENT | 400 mg CITRAPEAK® (glucosyl-hesperidin) supplementation | The active intervention consists of 400 mg of glucosyl-hesperidin (CITRAPEAK®) in capsule form. |
| DIETARY_SUPPLEMENT | Placebo | The placebo intervention consists of 400 mg/day of cellulose in capsule form, matching the appearance and dosage of active interventions. |
| DIETARY_SUPPLEMENT | 200 mg CITRAPEAK® (glucosyl-hesperidin) supplementation | The active intervention includes 200 mg of glucosyl-hesperidin (CITRAPEAK®) and an additional 200 mg of cellulose in capsule form. |
Timeline
- Start date
- 2025-04-15
- Primary completion
- 2026-01-01
- Completion
- 2026-01-01
- First posted
- 2024-11-04
- Last updated
- 2025-12-12
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT06672952. Inclusion in this directory is not an endorsement.