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Effect of a Botanical Ingredient in Healthy Subjects With Anxiety and Poor Sleep Quality

NCT06154629 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 79

Last updated 2024-02-16

No results posted yet for this study

Summary

Randomized, controlled, double-blind, single-center clinical trial with two parallel arms depending on the product consumed (experimental product and placebo product) to analyze the efficacy of a botanical extract in reducing anxiety and improving sleep quality.

Conditions

  • Poor Quality Sleep

Interventions

DIETARY_SUPPLEMENT

Botanical ingredient

Consumption for 90 days. Subjects should consume one capsule one hour before going to sleep

DIETARY_SUPPLEMENT

Control group

Consumption for 90 days. Subjects should consume one capsule one hour before going to sleep

Sponsors & Collaborators

  • Universidad Católica San Antonio de Murcia

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-09-15
Primary Completion
2023-12-22
Completion
2024-01-29

Countries

  • Spain

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06154629 on ClinicalTrials.gov