Curcumin and EGCG Supplementation to Improve Serum BDNF and Mood Disturbance

Part of paid clinical trials in Auburn, Alabama.

Sponsor
Auburn University
Study ID
NCT06531863
Phase
EARLY_PHASE1
Status
Recruiting

Conditions

  • Mood Disturbance

Eligibility Criteria

Sex
ALL
Age
18 Years - 50 Years
Healthy Volunteers
Accepted

Interventions

  • Curcumin — DIETARY_SUPPLEMENT
    1,330 mg curcumin
  • Epigallocatechin Gallate — DIETARY_SUPPLEMENT
    350 mg Epigallocatechin gallate (EGCG)
  • Placebo — OTHER
    Placebo to be consumed after randomization.

Study Details

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)

Key Dates

Start date
Sep 30, 2024
Status verified
Oct 2024
Primary completion
May 1, 2025
Completion
Aug 1, 2025

Study Design

Enrollment
64 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Experimental: Curcumin and EGCG Supplementation
    Participants in the intervention group with consume 1,330mg/day curcumin with 350mg/day EGCG.
  • Placebo Comparator: Placebo
    Participants will receive a placebo to consume everyday.

Primary Outcome Measure

Changes in total distress as measured via DASS-21 total score. [ Time Frame: 8-weeks ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Auburn University School of KinesiologyAuburnAlabama36849
Drew Fruge, PhD
3448448433

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