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NCT06531863 · ClinicalTrials.gov registry record · Early Phase 1

Curcumin and EGCG Supplementation to Improve Serum BDNF and Mood Disturbance

A Early Phase 1 study of Mood Disturbance, sponsored by Auburn University.

Recruiting
Registry status
Early Phase 1
Development phase
64
Enrollment target
1
Study location

NCT06531863: Recruiting Early Phase 1 study of Mood Disturbance, sponsored by Auburn University.

NCT06531863 is a Early Phase 1 study of Mood Disturbance that is actively recruiting participants, run by Auburn University. The registered enrollment target is 64 participants, above the 45-participant average among 3 other Mood Disturbance trials with a reported enrollment target (42% higher). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06531863, a Early Phase 1 study of Mood Disturbance, is actively recruiting participants, sponsored by Auburn University.

RECRUITING
Registry status
Early Phase 1
Development phase
64 participants
Enrollment target
1
Study location

Study Summary

The goal of this randomized placebo controlled trial is to examine mood disturbance and serum brain derived neurotrophic factor (BDNF) in people (age 18-50) with DASS-21 subscale scores \>9. The main questions it aims to answer are: Does curcumin and EGCG supplementation improve mood disturbance symptomology? Does curcumin and EGCG supplementation increase serum BDNF? Researchers will compare intervention versus placebo. Participants will consume an 8-week supplement of both: * 1,330mg/day curcumin * 350mg/day epigallocatechin gallate (EGCG)

Primary Outcome

The DASS-21 (Depression Anxiety and Stress Scale) Total ranges from 0 to 63, with lower numbers indicating less distress

Conditions Studied

Interventions

  • OTHER Placebo
  • DIETARY_SUPPLEMENT Curcumin
  • DIETARY_SUPPLEMENT Epigallocatechin Gallate

Study Locations (1)

Alabama

  • Auburn University School of Kinesiology - Auburn

Trial Details

FieldValue
Enrollment Target 64 participants
Start Date 2024-09-30
Est. Completion 2025-08-01
Phase Early Phase 1
Auburn University

54 total trials

What NCT06531863 shows while recruiting

NCT06531863 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 64 participants, a relatively small participant target, above the 45-participant average among 3 other Mood Disturbance trials with a reported enrollment target (42% higher).

The record links to 1 condition, with Mood Disturbance appearing as the primary indexed condition, and to 3 interventions - of which Placebo is the first listed.

NCT06531863 reports a single indexed study location in Alabama.

Frequently Asked Questions

What is clinical trial NCT06531863 about?

NCT06531863 is a clinical study titled "Curcumin and EGCG Supplementation to Improve Serum BDNF and Mood Disturbance". The goal of this randomized placebo controlled trial is to examine mood disturbance and serum brain derived neurotrophic factor (BDNF) in people (age 18-50) with DASS-21 subscale scores \>9. The main questions it aims to answer are: Does curcumin and EGCG supplementation improve mood disturbance sy...

What is the current status of trial NCT06531863?

This trial is currently recruiting. It is a Early Phase 1 study. The enrollment target is 64 participants. The study started on 2024-09-30. Estimated completion is 2025-08-01.

What conditions does trial NCT06531863 study?

This clinical trial studies the following conditions: Mood Disturbance.

What interventions are being tested in trial NCT06531863?

The interventions under investigation include: Placebo (OTHER), Curcumin (DIETARY_SUPPLEMENT), Epigallocatechin Gallate (DIETARY_SUPPLEMENT).

Who is sponsoring clinical trial NCT06531863?

This trial is sponsored by Auburn University, which has 54 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06531863 being conducted?

This trial has 1 study location across Alabama. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Mood Disturbance

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

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Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

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Source: ClinicalTrials.gov NCT06531863, the US trial registry maintained by the National Library of Medicine. NCT06531863 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.