Effects of Cistanche Supplementation on Anaerobic Exercise Performance and Recovery in Men With Different Athletic Training Levels

April 20, 2026 updated by: Beijing Sport University

Effects of Cistanche Supplementation on Anaerobic Exercise Performance and Recovery in Men With Different Athletic Training Levels: A Double-Blind, Randomized, Placebo-Controlled Trial

This study is a double-blind, randomized, placebo-controlled trial designed to examine whether 8 weeks of Cistanche deserticola supplementation, when combined with a standardized anaerobic training program, can improve anaerobic exercise performance, recovery, and selected body composition outcomes in young adult men with different athletic training levels.

Participants will be assigned to receive either Cistanche deserticola extract or a matched placebo while completing the same supervised anaerobic training program. The study will assess changes in anaerobic performance, including Wingate test outcomes and jump performance, as well as recovery-related indicators such as blood lactate, creatine kinase, malondialdehyde, testosterone, cortisol, and the testosterone-to-cortisol ratio. Body composition outcomes, including body fat percentage and skeletal muscle mass, will also be evaluated.

The purpose of this study is to determine whether Cistanche deserticola supplementation provides additional benefits beyond training alone, and whether these effects differ between highly trained and recreationally trained participants.

Study Overview

Study Type

Interventional

Enrollment (Actual)

56

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Hubei
      • Wuhan, Hubei, China, 430000
        • Wuhan Sport University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Male, aged 18 to 25 years
  • Body mass index (BMI) between 18.5 and 25.0 kg/m²
  • Able and willing to provide written informed consent
  • Willing to comply with study procedures, supplementation, training, and assessments
  • Belonging to one of the following athletic training strata:
  • High-level elite stratum: Chinese National Level-1 Athlete standard in sprint-related events, regular training in past 12 months and active during study
  • Amateur stratum: regular exercise-training background in past 12 months without National Level-1 status

Exclusion Criteria:

  • Use of steroids or ergogenic supplements during study
  • Known cardiovascular, metabolic, musculoskeletal, or other conditions making participation unsafe or affecting outcomes
  • Current use of medications affecting muscle growth, recovery, hormones, or high-intensity performance
  • Current injury or limitation preventing safe participation
  • Known allergy or intolerance to supplement/placebo ingredients
  • Participation in another clinical trial or structured intervention during study period
  • Inability or unwillingness to comply with protocol
  • Any other condition deemed unsuitable by investigators

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Health Services Research
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Cistanche Supplementation + Standardized Anaerobic Training
Participants in this arm receive Cistanche deserticola extract paste (5 g/day) for 8 weeks while completing the same supervised standardized anaerobic training program as the control arm. The training program is performed 3 times per week and includes repeated sprint training, explosive/strength-support exercises, and short-bout high-intensity interval training.
Participants receive Cistanche deserticola extract paste at a dose of 5 g/day for 8 weeks. The supplement is administered in two sachets per day, one after breakfast and one after lunch. The product is derived from Cistanche deserticola Y.C. Ma cultivated in Inner Mongolia and consists primarily of phenylethanoid glycosides. Batch-specific quality-control documentation is provided by the supplier to ensure consistency.
All participants complete the same supervised standardized anaerobic training program 3 times per week for 8 consecutive weeks. Each session lasts approximately 50 to 65 minutes and includes a dynamic warm-up, repeated sprint training, explosive/strength-support exercises, short-bout high-intensity interval training, and a cool-down. Training load is progressively increased across the intervention period, and attendance as well as session rating of perceived exertion are recorded throughout the study.
Active Comparator: Placebo + Standardized Anaerobic Training
Participants in this arm receive a matched placebo for 8 weeks while completing the same supervised standardized anaerobic training program as the experimental arm. The placebo is matched in appearance, weight, texture, and taste. The training program is performed 3 times per week and includes repeated sprint training, explosive/strength-support exercises, and short-bout high-intensity interval training.
All participants complete the same supervised standardized anaerobic training program 3 times per week for 8 consecutive weeks. Each session lasts approximately 50 to 65 minutes and includes a dynamic warm-up, repeated sprint training, explosive/strength-support exercises, short-bout high-intensity interval training, and a cool-down. Training load is progressively increased across the intervention period, and attendance as well as session rating of perceived exertion are recorded throughout the study.
Participants receive a matched placebo for 8 weeks. The placebo is administered in two sachets per day, one after breakfast and one after lunch, following the same schedule as the experimental supplement. It contains maltodextrin, microcrystalline cellulose, caramel coloring, and a food-grade bittering agent, and is matched to the active supplement in appearance, weight, texture, and taste.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Peak power during the 30-second Wingate Anaerobic Test
Time Frame: Baseline (week 0) and post-intervention (week 8)
Peak power (W) measured during a 30-second Wingate Anaerobic Test performed on a Monark 894E cycle ergometer. The test is conducted under standardized conditions, and the primary analysis will evaluate the change from baseline to post-intervention and the between-group difference in change after 8 weeks of intervention.
Baseline (week 0) and post-intervention (week 8)
Squat jump height
Time Frame: Baseline (week 0) and post-intervention (week 8)
Squat jump (SJ) height in centimeters, assessed under standardized testing conditions as a measure of lower-limb explosive performance. Analyses will assess change from baseline to post-intervention and between-group differences in change.
Baseline (week 0) and post-intervention (week 8)
Countermovement jump
Time Frame: Baseline (week 0) and post-intervention (week 8)
Countermovement jump (CMJ) height in centimeters, assessed under standardized testing conditions as a measure of lower-limb explosive performance. Analyses will assess change from baseline to post-intervention and between-group differences in change.
Baseline (week 0) and post-intervention (week 8)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Average power during the 30-second Wingate Anaerobic Test
Time Frame: Baseline (week 0) and post-intervention (week 8)
Average power (W) measured during the 30-second Wingate Anaerobic Test. Analyses will assess change from baseline to post-intervention and between-group differences in change.
Baseline (week 0) and post-intervention (week 8)
Minimum power during the 30-second Wingate Anaerobic Test
Time Frame: Baseline (week 0) and post-intervention (week 8)
Baseline (week 0) and post-intervention (week 8)
Power drop during the 30-second Wingate Anaerobic Test
Time Frame: Baseline (week 0) and post-intervention (week 8)
Power drop (%) calculated from the 30-second Wingate Anaerobic Test as an index of fatigue during maximal anaerobic effort. Analyses will assess change from baseline to post-intervention and between-group differences in change.
Baseline (week 0) and post-intervention (week 8)
Post-exercise blood lactate response
Time Frame: Baseline (week 0) and post-intervention (week 8)
Capillary blood lactate concentration (mmol/L) measured immediately after the Wingate Anaerobic Test and at 3 minutes of recovery as indices of acute metabolic stress and recovery. Analyses will assess change from baseline to post-intervention and between-group differences in change.
Baseline (week 0) and post-intervention (week 8)
Serum creatine kinase concentration
Time Frame: Baseline (week 0) and post-intervention (week 8)
Baseline (week 0) and post-intervention (week 8)
Serum malondialdehyde concentration
Time Frame: Baseline (week 0) and post-intervention (week 8)
Serum malondialdehyde (MDA, nmol/mL) measured as a biomarker related to oxidative stress. Analyses will assess change from baseline to post-intervention and between-group differences in change.
Baseline (week 0) and post-intervention (week 8)
Serum testosterone concentration
Time Frame: Baseline (week 0) and post-intervention (week 8)
Fasting serum testosterone concentration (ng/mL) measured from venous blood samples collected under standardized morning conditions.
Baseline (week 0) and post-intervention (week 8)
Body fat percentage
Time Frame: Baseline (week 0) and post-intervention (week 8)
Body fat percentage measured using bioelectrical impedance analysis (InBody 770). Analyses will assess change from baseline to post-intervention and between-group differences in change.
Baseline (week 0) and post-intervention (week 8)
Skeletal muscle mass
Time Frame: Baseline (week 0) and post-intervention (week 8)
Skeletal muscle mass (kg) measured using bioelectrical impedance analysis (InBody 770). Analyses will assess change from baseline to post-intervention and between-group differences in change.
Baseline (week 0) and post-intervention (week 8)
Serum cortisol concentration
Time Frame: Baseline (week 0) and post-intervention (week 8)
Fasting serum cortisol concentration (μg/dL) measured from venous blood samples collected under standardized morning conditions.
Baseline (week 0) and post-intervention (week 8)

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Body mass index
Time Frame: Baseline (week 0) and post-intervention (week 8)
Body mass index (BMI, kg/m²) calculated from measured height and body weight.
Baseline (week 0) and post-intervention (week 8)
Body weight
Time Frame: Baseline (week 0) and post-intervention (week 8)
Body weight (kg) measured under standardized fasting conditions. Analyses will assess change from baseline to post-intervention and between-group differences in change.
Baseline (week 0) and post-intervention (week 8)
Resting blood lactate concentration
Time Frame: Baseline (week 0) and post-intervention (week 8)
Capillary blood lactate concentration (mmol/L) measured before the Wingate Anaerobic Test under resting conditions. Analyses will assess change from baseline to post-intervention and between-group differences in change.
Baseline (week 0) and post-intervention (week 8)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

November 20, 2025

Primary Completion (Actual)

April 1, 2026

Study Completion (Actual)

April 12, 2026

Study Registration Dates

First Submitted

April 13, 2026

First Submitted That Met QC Criteria

April 20, 2026

First Posted (Actual)

April 22, 2026

Study Record Updates

Last Update Posted (Actual)

April 22, 2026

Last Update Submitted That Met QC Criteria

April 20, 2026

Last Verified

April 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

IPD Plan Description

The investigators have not yet decided whether individual participant data will be shared. Any future sharing of de-identified data will depend on participant consent, institutional requirements, ethics approval, and data governance considerations.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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