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 Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
DOUBLE
Enrollment
56
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.
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.
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.
Wuhan Sport University
Wuhan, Hubei, China
Peak power during the 30-second Wingate Anaerobic Test
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.
Time frame: Baseline (week 0) and post-intervention (week 8)
Squat jump height
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.
Time frame: Baseline (week 0) and post-intervention (week 8)
Countermovement jump
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.
Time frame: Baseline (week 0) and post-intervention (week 8)
Average power during the 30-second Wingate Anaerobic Test
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.
Time frame: 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)
Power drop during the 30-second Wingate Anaerobic Test
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.
Time frame: Baseline (week 0) and post-intervention (week 8)
Post-exercise blood lactate response
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.
Time frame: Baseline (week 0) and post-intervention (week 8)
Serum creatine kinase concentration
Time frame: Baseline (week 0) and post-intervention (week 8)
Serum malondialdehyde concentration
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.
Time frame: Baseline (week 0) and post-intervention (week 8)
Serum testosterone concentration
Fasting serum testosterone concentration (ng/mL) measured from venous blood samples collected under standardized morning conditions.
Time frame: Baseline (week 0) and post-intervention (week 8)
Body fat percentage
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.
Time frame: Baseline (week 0) and post-intervention (week 8)
Skeletal muscle mass
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.
Time frame: Baseline (week 0) and post-intervention (week 8)
Serum cortisol concentration
Fasting serum cortisol concentration (μg/dL) measured from venous blood samples collected under standardized morning conditions.
Time frame: Baseline (week 0) and post-intervention (week 8)
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