AzTrials
AzTrials

Exercise PhysiologyNCT07268976

Jackfruit Effects on Adipokines and Cognition in Boxers

A study testing Jackfruit Supplement in people with Exercise Physiology and Cognitive Function, run by Bayburt University at 1 site in Turkey (Türkiye).

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
Search all trials

Trial summary

This study investigates the effects of jackfruit oil extract on adipokine levels (Irisin, Omentin-1), brain-derived neurotrophic factor (BDNF), cognitive performance, and body measurements in healthy young boxers aged 18-25. Read more about this study

Who is it for?
Ages 18 to 25 yearsHealthy volunteers can take part
What is being tested?
Jackfruit Supplement
Type of treatment
Pill or oral medicine
Could I receive a placebo?
No, everyone receives an active treatment
How many people
30 participants
Where
1 siteTurkey (Türkiye)
Study dates
7 Jan 2025to 10 Jun 2025
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 25 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Male boxers aged 18-25 years
  • Healthy individuals without any diagnosed chronic disease
  • Participating in regular weekly boxing training
  • Able to continue training throughout the study period
  • Willing to voluntarily participate in the study
  • Able to provide written and/or verbal informed consent

Who cannot join

  • Presence of chronic diseases (e.g., diabetes, cardiovascular disorders)
  • Any injury or musculoskeletal condition preventing continuation of training
  • Known allergy or hypersensitivity to jackfruit or its components
  • Use of medications or supplements that could interfere with study outcomes
  • Individuals who refuse to provide informed consent

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • Bayburt Gençlik Merkezi Kapali Spor Salonu

    Bayburt, Merkez, 69000

Other trials in Turkey (Türkiye)

About this study

Official title: Effect of Jackfruit Consumption on Adipokine, Cerebral Response, Cognitive Performance and Anthropometric Parameters in Boxers

This study investigates the effects of jackfruit oil extract on adipokine levels (Irisin, Omentin-1), brain-derived neurotrophic factor (BDNF), cognitive performance, and body measurements in healthy young boxers aged 18-25. Participants were randomly assigned to four groups receiving different doses of jackfruit oil extract (0, 100, 200, 300 mg/kg) or no supplement. Saliva samples, cognitive tests, and body measurements were collected at the start of the study and after 30 days to evaluate the outcomes.

Read the detailed description

This interventional study evaluates the effects of different doses of jackfruit oil extract on healthy young boxers aged 18-25. Participants were randomly assigned to four groups and followed for 30 days.

Saliva samples were collected to measure irisin, omentin-1, and BDNF levels. Cognitive performance was assessed using the Wisconsin Card Sorting Test and the Trail Making Test. Anthropometric parameters including weight, BMI, waist, hip, chest, limb circumferences, and body composition were measured at baseline and on day 30.

Statistical analyses were performed using SPSS version 26. ANOVA, Duncan, and Pearson correlation tests were used to determine significant differences and relationships between variables.

This study is randomized and controlled. Participants receive either one of three doses of jackfruit oil extract or no supplement. The follow-up period is 30 days.

Being tested
Jackfruit Supplement
Keywords
Boxer, Athletes, Jackfruit, Irisin, Omentin-1, BDNF, Cognitive Performance, Anthropometric Measurements, Adipokines, Trail Making Test, Wisconsin Card Sorting Test (WCST), Body Composition

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Jackfruit SupplementDietary supplement

    Participants in the experimental group will receive a daily dose of jackfruit supplement during the study period. The supplement is administered orally and standardized for bioactive components. Participants in the control group will not receive any jackfruit supplement.

Study groups in NCT07268976
Study groupRoleWhat they receive
J0 - Kontrol GrubuNo interventionKatılımcılar hiçbir jackfruit yağı ekstresi almadı. Sadece normal diyet ve antrenman programlarını sürdürdüler.
J100ExperimentalKatılımcılara 100 mg/kg jackfruit yağı ekstresi oral olarak 500 ml su içinde verildi. Müdahale 30 gün boyunca günlük olarak uygulandı.
Receives: Dietary Supplement: Jackfruit Supplement
J200ExperimentalKatılımcılara 200 mg/kg jackfruit yağı ekstresi oral olarak 500 ml su içinde verildi. Müdahale 30 gün boyunca günlük olarak uygulandı.
Receives: Dietary Supplement: Jackfruit Supplement
J300ExperimentalKatılımcılara 300 mg/kg jackfruit yağı ekstresi oral olarak 500 ml su içinde verildi. Müdahale 30 gün boyunca günlük olarak uygulandı.
Receives: Dietary Supplement: Jackfruit Supplement

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Salivary Irisin Level

    Irisin levels measured from saliva samples collected from participants using the ELISA method.

    Measured: Day 0 and Day 30

  2. Salivary Omentin-1 Level

    Omentin-1 levels measured from saliva samples collected from participants using the ELISA method.

    Measured: Day 0 and Day 30.

  3. Salivary BDNF Level

    BDNF levels measured from saliva samples collected from participants using the ELISA method.

    Measured: Day 0 and Day 30.

Secondary outcomes (28)
  1. Body Weight (kg)

    Body weight measured using Tanita BC-418 bioimpedance device.

    Measured: Day 0 and Day 30

  2. Height (cm)

    Height measured using a standard stadiometer.

    Measured: Day 0 and Day 30

  3. Body Mass Index (kg/m²)

    BMI calculated using the formula weight (kg)/height (m²).

    Measured: Day 0 and Day 30

  4. Waist Circumference (cm)

    Waist circumference measured with a flexible tape measure.

    Measured: Day 0 and Day 30

  5. Hip Circumference (cm)

    Hip circumference measured with a flexible tape measure.

    Measured: Day 0 and Day 30

  6. Chest Circumference (cm)

    Chest circumference measured using a flexible tape measure.

    Measured: Day 0 and Day 30

  7. Upper Arm Circumference (Right/Left, cm)

    Right and left upper arm circumferences measured with a flexible tape measure.

    Measured: Day 0 and Day 30

  8. Wrist Circumference (Right/Left, cm)

    Right and left wrist circumferences measured with a flexible tape measure.

    Measured: Day 0 and Day 30

  9. Thigh Circumference (Right/Left, cm)

    Right and left thigh circumferences measured with a flexible tape measure.

    Measured: Day 0 and Day 30

  10. Calf Circumference (Right/Left, cm)

    Right and left calf circumferences measured with a flexible tape measure.

    Measured: Day 0 and Day 30

  11. Total Body Fat Mass (kg)

    Total body fat mass measured using Tanita BC-418.

    Measured: Day 0 and Day 30

  12. Total Body Fat Percentage (%)

    Total body fat percentage measured using Tanita BC-418.

    Measured: Day 0 and Day 30

  13. Abdominal Fat Mass (kg)

    Abdominal fat mass measured using Tanita BC-418.

    Measured: Day 0 and Day 30

  14. Regional Fat Percentages (Right/Left Arm & Leg)

    Regional fat percentages for arms and legs measured by Tanita BC-418.

    Measured: Day 0 and Day 30

  15. Total Muscle Mass (kg)

    Total muscle mass assessed using Tanita BC-418.

    Measured: Day 0 and Day 30

  16. Regional Muscle Mass (Right/Left Arm & Leg, kg)

    Regional muscle mass of arms and legs measured by Tanita BC-418.

    Measured: Day 0 and Day 30

  17. Basal Metabolic Rate (BMR)

    Basal metabolic rate calculated by Tanita BC-418.

    Measured: Day 0 and Day 30

  18. Metabolic Age

    Metabolic age estimated using Tanita BC-418 device.

    Measured: Day 0 and Day 30

  19. Total Body Water (kg)

    Total body water measured via bioimpedance analysis.

    Measured: Day 0 and Day 30

  20. Total Body Water Percentage (%)

    Total Body Water Percentage (%)

    Measured: Day 0 and Day 30

  21. WCST Total Correct Responses

    Total correct responses obtained from the Wisconsin Card Sorting Test.

    Measured: Day 0 and Day 30

  22. WCST Total Incorrect Responses

    Total incorrect responses measured using the Wisconsin Card Sorting Test.

    Measured: Day 0 and Day 30

  23. WCST Perseverative Error Count

    Perseverative errors recorded during the Wisconsin Card Sorting Test.

    Measured: Day 0 and Day 30

  24. WCST Total Time (seconds)

    Total time required to complete the Wisconsin Card Sorting Test.

    Measured: Day 0 and Day 30

  25. Trail Making Test A Completion Time (seconds)

    Completion time for Trail Making Test Part A.

    Measured: Day 0 and Day 30

  26. Trail Making Test B Completion Time (seconds)

    Completion time for Trail Making Test Part B.

    Measured: Day 0 and Day 30

  27. Biomarker Correlations (Irisin-Omentin-BDNF vs. Dose/Day)

    Pearson correlation analysis examining relationships between biomarkers and intervention dose/day.

    Measured: Based on Day 30 measurements

  28. Safety Outcomes (Adverse Event Monitoring)

    Monitoring of potential adverse events related to 300 mg/kg JOE administration.

    Measured: Continuous monitoring throughout 30 days

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted8 Dec 2025
  2. Study start7 Jan 2025
  3. Primary completion10 Feb 2025
  4. Study completion10 Jun 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Other
Allocation
Randomised
Intervention model
Parallel groups
Model description
Participants were randomly assigned to four parallel groups (J0, J100, J200, J300) receiving different doses of jackfruit oil extract (0, 100, 200, 300 mg/kg). Each group received the assigned intervention for 30 days, and outcomes including salivary irisin, omentin-1, BDNF levels, cognitive performance, and anthropometric measurements were assessed at baseline and at the end of the intervention.
Masking
None (open label)
Enrolment
30 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07268976
Sponsor's protocol ID
BU-2025-01
Status last verified
Dec 2025
First submitted
26 Aug 2025
Last updated
8 Dec 2025
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: De-identified participant-level data including salivary irisin, omentin-1, BDNF levels, anthropometric measurements, and cognitive test results will be shared with other researchers upon reasonable request after publication of the main study results. Access will require approval from the institutional ethics committee and signing a data use agreement.

Questions about this trial

What is this clinical trial studying?

A study testing Jackfruit Supplement in people with Exercise Physiology and Cognitive Function, run by Bayburt University at 1 site in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 8 Dec 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Salivary Irisin Level (time frame: Day 0 and Day 30). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 8 Dec 2025.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in