CClinicalTrials.gg
CompletedNCT07398248PLBT-ATHUpdated Feb 9, 2026

Effects of Powerlifting-Based Training in Athletes

An interventional study of Powerlifting-Based Training and Usual Basketball Training in Physical Fitness, Hormonal Response and Metabolic Parameters, sponsored by Ramazan Erdoğan. Completed at 2 sites in Turkey (Türkiye). Open to male participants aged 18 Years to 24 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-02-09.

Sponsored by Ramazan Erdoğan · Not applicable, Interventional, and Other

From the registry’s dates

  • Registered 11 months after the study started (first participant enrolled Jan 2025, registered Dec 2025).
Phase
Not applicable
Study type
Interventional
Enrollment
30
Allocation
Randomized
Ages
18 Years to 24 Years
Sex
Male
01

Study summary

This randomized controlled trial aims to examine the effects of a weightlifting-based training program on hormonal, metabolic, and lipid profile parameters in athletes. Participants will be randomly assigned to either a weightlifting-based training group or a control group. The training program will be implemented for a specific period, and relevant blood parameters will be evaluated before and after the intervention. The findings of this study may contribute to a better understanding of the physiological effects of weightlifting-based training on athletes.

Read the detailed description

This study is designed as a randomized controlled trial to investigate the effects of a structured weightlifting training program on hormonal, metabolic, and lipid profile parameters in athletes. Eligible participants will be randomly assigned to either an intervention group undergoing a weightlifting-based training protocol or a control group continuing their usual training routines.

The intervention will be implemented over a predetermined training period, and outcome measures will include selected hormonal, metabolic, and lipid profile markers obtained from blood samples. Measurements will be taken at baseline and at the end of the training period. The results of this study are expected to provide evidence on physiological adaptations associated with weightlifting-based training and offer practical implications for training program design in athletic populations.

02

Conditions studied

  • Physical Fitness
  • Hormonal Response
  • Metabolic Parameters

Keywords

  • Powerlifting
  • Strength Training
  • Basketball
03

In context

Lead sponsor

This is the only study on the registry with Ramazan Erdoğan as lead sponsor.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 24 Years
Sexes eligible
Male
Accepts healthy volunteers
Yes

Inclusion criteria

  • Male basketball players aged 18 to 24 years
  • At least two years of regular sports experience
  • Actively participating in basketball training and competition
  • Voluntary participation with written informed consent

Exclusion criteria

Exclusion Criteria:

  • History of musculoskeletal injury or surgery within the last six months
  • Presence of chronic disease or metabolic disorder
  • Use of performance-enhancing drugs or hormonal supplements
  • Participation in another structured training program during the study period
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
30 participants (actual)

Study arms

  • Experimental
    Powerlifting-Based Training Group

    Participants performed a structured powerlifting-based training program in addition to their regular basketball training. The intervention was conducted three days per week for six weeks. Each session lasted approximately 60 minutes and included a standardized warm-up, a powerlifting-focused main training phase, and a cool-down period. The training program emphasized the squat, bench press, and deadlift exercises performed with progressive intensity. Accessory exercises targeting lower-body strength, upper-body musculature, and core stability were included. High-intensity bodyweight exercises were also performed to enhance anaerobic capacity and neuromuscular performance. All training sessions were supervised by qualified staff.

    Other: Powerlifting-Based Training · Other: Blood Sampling and Laboratory Analysis

  • Other
    Control Group

    Participants continued their usual basketball training routines throughout the study period without any additional strength or powerlifting-based exercises.

    Other: Usual Basketball Training · Other: Blood Sampling and Laboratory Analysis

Interventions

  • OtherPowerlifting-Based Training

    Participants will perform a structured powerlifting-based training program including squat, bench press, and deadlift exercises, conducted 3 sessions per week for 8 weeks under supervision.

  • OtherUsual Basketball Training

    Participants continued their usual basketball training routines without any additional strength or powerlifting-based exercises.

  • OtherBlood Sampling and Laboratory Analysis

    Venous blood samples were collected from participants at baseline and post-intervention following an overnight fast. Hormonal parameters were analyzed using ELISA methods, and metabolic and lipid profile parameters were analyzed using an automated biochemical analyzer.

06

What researchers measure

Primary outcomes

  1. Mean Change in Fasting Serum Total Testosterone Concentration Measured by ELISA (ng/dL)

    Mean difference between baseline and post-intervention fasting serum total testosterone concentrations, measured from venous blood samples using a commercially available enzyme-linked immunosorbent assay (ELISA).

    Time frame: Baseline and post-intervention (8 weeks)

  2. Mean Change in Fasting Serum Cortisol Concentration Measured by ELISA (µg/dL)

    Mean difference between baseline and post-intervention fasting serum cortisol concentrations, measured from venous blood samples using a commercially available enzyme-linked immunosorbent assay (ELISA).

    Time frame: Baseline and post-intervention (8 weeks)

  3. Mean Change in Fasting Serum Growth Hormone Concentration Measured by ELISA (ng/mL)

    Mean difference between baseline and post-intervention fasting serum growth hormone concentrations, measured from venous blood samples using a commercially available enzyme-linked immunosorbent assay (ELISA).

    Time frame: Baseline and post-intervention (8 weeks)

  4. Mean Change in Fasting Serum Thyroid-Stimulating Hormone Concentration Measured by ELISA (µIU/mL)

    Mean difference between baseline and post-intervention fasting serum thyroid-stimulating hormone concentrations, measured from venous blood samples using a commercially available enzyme-linked immunosorbent assay (ELISA).

    Time frame: Baseline and post-intervention (8 weeks)

  5. Mean Change in Fasting Serum Triiodothyronine Concentration Measured by ELISA (ng/dL)

    Mean difference between baseline and post-intervention fasting serum triiodothyronine concentrations, measured from venous blood samples using a commercially available enzyme-linked immunosorbent assay (ELISA).

    Time frame: Baseline and post-intervention (8 weeks)

  6. Mean Change in Fasting Serum Thyroxine Concentration Measured by ELISA (µg/dL)

    Mean difference between baseline and post-intervention fasting serum thyroxine concentrations, measured from venous blood samples using a commercially available enzyme-linked immunosorbent assay (ELISA).

    Time frame: Baseline and post-intervention (8 weeks)

Secondary outcomes

  1. Mean Change in Fasting Serum Insulin Concentration Measured by ELISA (µIU/mL)

    Mean difference between baseline and post-intervention fasting serum insulin concentrations, measured from venous blood samples using a commercially available enzyme-linked immunosorbent assay (ELISA).

    Time frame: Baseline and post-intervention (8 weeks)

  2. Mean Change in Fasting Blood Glucose Concentration Measured by Automated Biochemical Analyzer (mg/dL)

    Mean difference between baseline and post-intervention fasting blood glucose concentrations, measured from venous blood samples using an automated biochemical analyzer.

    Time frame: Baseline and post-intervention (8 weeks)

  3. Mean Change in Total Cholesterol Concentration Measured by Automated Biochemical Analyzer (mg/dL)

    Mean difference between baseline and post-intervention total cholesterol concentrations, measured from venous blood samples using an automated biochemical analyzer.

    Time frame: Baseline and post-intervention (8 weeks)

  4. Mean Change in Low-Density Lipoprotein Cholesterol Concentration Measured by Automated Biochemical Analyzer (mg/dL)

    Mean difference between baseline and post-intervention low-density lipoprotein cholesterol concentrations, measured from venous blood samples using an automated biochemical analyzer.

    Time frame: Baseline and post-intervention (8 weeks)

  5. Mean Change in High-Density Lipoprotein Cholesterol Concentration Measured by Automated Biochemical Analyzer (mg/dL)

    Mean difference between baseline and post-intervention high-density lipoprotein cholesterol concentrations, measured from venous blood samples using an automated biochemical analyzer.

    Time frame: Baseline and post-intervention (8 weeks)

  6. Mean Change in Triglyceride Concentration Measured by Automated Biochemical Analyzer (mg/dL)

    Mean difference between baseline and post-intervention triglyceride concentrations, measured from venous blood samples using an automated biochemical analyzer.

    Time frame: Baseline and post-intervention (8 weeks)

07

Study locations

2 sites
  • Faculty of Sport Sciences
    Tunceli, Center 62000, Turkey (Türkiye)
  • Munzur University
    Bitlis, Tunceli 62000, Turkey (Türkiye)
08

References and documents

Publications

  • Tizar E, Erdogan R. Short-term effects of powerlifting-based training on hormonal, metabolic, and lipid profile markers in male basketball players: a randomized controlled trial. BMC Sports Sci Med Rehabil. 2026 Jul 1. doi: 10.1186/s13102-026-01832-4. Online ahead of print. PubMed 42387653 ↗

Study documents

  • Study protocol · Sep 9, 2025

Documents are hosted by the registry — open the source record to download them.

Individual participant data

Plan to share: No — Individual participant data will not be shared due to ethical restrictions, participant confidentiality concerns, and the absence of participant consent for data sharing beyond the scope of this study.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 9, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07398248
Lead sponsor
Ramazan Erdoğan
Responsible party
Ramazan Erdoğan (Associate Professor, Munzur University) — Sponsor-investigator
First posted
Feb 9, 2026
Start date
Jan 10, 2025
Primary completion
Jun 15, 2025
Completion
Oct 15, 2025
Last update
Feb 9, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Jan 2026. You cannot join it, but the record below documents what was studied.

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