Effects of NR Supplementation on Metabolic Flexibility in Zone 2 Training

NCT ID: NCT07344636

Last Updated: 2026-01-15

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

16 participants

Study Classification

INTERVENTIONAL

Study Start Date

2026-01-31

Study Completion Date

2027-07-31

Brief Summary

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Zone 2 training, a low-intensity endurance exercise performed at approximately 66-80% of VO₂max or near the first ventilatory threshold, has gained popularity for improving aerobic capacity, fat metabolism, and mitochondrial efficiency. It preserves glycogen stores and delays fatigue, making it an essential training method for both athletes and recreational exercisers. Nicotinamide adenine dinucleotide (NAD) is a vital metabolite that regulates cellular energy metabolism and redox homeostasis. It participates in oxidative reactions within the tricarboxylic acid cycle and electron transport chain, sustaining ATP synthesis and mitochondrial efficiency. Exercise influences multiple pathways of NAD metabolism, altering the NAD⁺/NADH ratio and thereby affecting energy production and fatigue resistance. Studies have shown that both aerobic exercise and NAD precursor supplementation (e.g., nicotinamide riboside \[NR\]) can elevate body NAD levels and enhance mitochondrial function, though findings remain inconsistent due to variations in dosage and participants' characteristics. This study aims to investigate how acute NR supplementation interacts with Zone 2 cycling training in adults. Specifically, it examines the temporal and dose-dependent effects of NR supplementation on metabolic flexibility and exercise performance. The results may clarify the potential synergistic benefits of combining NAD supplementation with low-intensity endurance training to improve aerobic adaptability.

Detailed Description

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Conditions

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Health Adult Subjects

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

OTHER

Blinding Strategy

DOUBLE

Participants Outcome Assessors

Study Groups

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600 mg

Group Type EXPERIMENTAL

Nicotinamide Riboside (NR)

Intervention Type DIETARY_SUPPLEMENT

600 mg NR

300 mg

Group Type EXPERIMENTAL

Nicotinamide Riboside (NR)

Intervention Type DIETARY_SUPPLEMENT

300 mg NR

0 mg

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Nicotinamide Riboside (NR)

600 mg NR

Intervention Type DIETARY_SUPPLEMENT

Nicotinamide Riboside (NR)

300 mg NR

Intervention Type DIETARY_SUPPLEMENT

Eligibility Criteria

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Inclusion Criteria

* Over 18 years old
* BMI \<30 kg/m2

Exclusion Criteria

* Present of health conditions that contraindicate participation in exercise training, such as a history of cardiovascular disease, cancer, or musculoskeletal disorders
* Currently taking vitamin B supplements and/or NAD precursors
* Taking medication that may affect the test results
Minimum Eligible Age

18 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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ZHANG Jiaqi

OTHER

Sponsor Role lead

Responsible Party

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ZHANG Jiaqi

Principal Investigator

Responsibility Role SPONSOR_INVESTIGATOR

Other Identifiers

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SBRE-25-0349

Identifier Type: -

Identifier Source: org_study_id

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