NCT07268976

Brief 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. 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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
30

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Jan 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 7, 2025

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 10, 2025

Completed
4 months until next milestone

Study Completion

Last participant's last visit for all outcomes

June 10, 2025

Completed
3 months until next milestone

First Submitted

Initial submission to the registry

August 26, 2025

Completed
3 months until next milestone

First Posted

Study publicly available on registry

December 8, 2025

Completed
Last Updated

December 8, 2025

Status Verified

December 1, 2025

Enrollment Period

1 month

First QC Date

August 26, 2025

Last Update Submit

December 4, 2025

Conditions

Keywords

BoxerAthletesJackfruitIrisinOmentin-1BDNFCognitive PerformanceAnthropometric MeasurementsAdipokinesTrail Making TestWisconsin Card Sorting Test (WCST)Body Composition

Outcome Measures

Primary Outcomes (3)

  • Salivary Irisin Level

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

    Day 0 and Day 30

  • Salivary Omentin-1 Level

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

    Day 0 and Day 30.

  • Salivary BDNF Level

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

    Day 0 and Day 30.

Secondary Outcomes (28)

  • Body Weight (kg)

    Day 0 and Day 30

  • Height (cm)

    Day 0 and Day 30

  • Body Mass Index (kg/m²)

    Day 0 and Day 30

  • Waist Circumference (cm)

    Day 0 and Day 30

  • Hip Circumference (cm)

    Day 0 and Day 30

  • +23 more secondary outcomes

Study Arms (4)

J0 - Kontrol Grubu

NO INTERVENTION

Katılımcılar hiçbir jackfruit yağı ekstresi almadı. Sadece normal diyet ve antrenman programlarını sürdürdüler.

J100

EXPERIMENTAL

Katılımcılara 100 mg/kg jackfruit yağı ekstresi oral olarak 500 ml su içinde verildi. Müdahale 30 gün boyunca günlük olarak uygulandı.

Dietary Supplement: Jackfruit Supplement

J200

EXPERIMENTAL

Katılımcılara 200 mg/kg jackfruit yağı ekstresi oral olarak 500 ml su içinde verildi. Müdahale 30 gün boyunca günlük olarak uygulandı.

Dietary Supplement: Jackfruit Supplement

J300

EXPERIMENTAL

Katılımcılara 300 mg/kg jackfruit yağı ekstresi oral olarak 500 ml su içinde verildi. Müdahale 30 gün boyunca günlük olarak uygulandı.

Dietary Supplement: Jackfruit Supplement

Interventions

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.

J100J200J300

Eligibility Criteria

Age18 Years - 25 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • 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

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Bayburt Gençlik Merkezi Kapali Spor Salonu

Bayburt, Merkez, 69000, Turkey (Türkiye)

Location

Related Links

Study Officials

  • BÜLENT BAYRAKTAR

    BAYBURT ÜNİVERSİTESİ

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
OTHER
Intervention Model
PARALLEL
Model Details: 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.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Researcher / Principal Investigator/ Master's Student

Study Record Dates

First Submitted

August 26, 2025

First Posted

December 8, 2025

Study Start

January 7, 2025

Primary Completion

February 10, 2025

Study Completion

June 10, 2025

Last Updated

December 8, 2025

Record last verified: 2025-12

Data Sharing

IPD Sharing
Will share

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.

Shared Documents
STUDY PROTOCOL, SAP, ANALYTIC CODE
Time Frame
De-identified participant-level data and supporting documents will be available to other researchers starting after publication of the main study results and will remain accessible for 5 years following publication.
Access Criteria
"Access to de-identified participant-level data and supporting documents will be granted to qualified researchers for legitimate scientific purposes. Researchers must submit a request detailing their research objectives and methods, obtain approval from the institutional ethics committee, and sign a data use agreement. Approved researchers will receive access to the specified datasets and supporting materials electronically.
More information

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