Black Cumin Seed Oil's Impact on Stress and Quality of Life in Moderately-Stressed Adults
black cumin seed oil
Supportive Care Study
Summary
Study start date: April 1, 2025
Actual date on which the first participant was enrolled.This study investigates the potential benefits of black cumin seed oil, a natural substance used for centuries in traditional medicine, on stress levels and overall quality of life in healthy adults who are experiencing moderate stress. The oil, known for its active ingredient thymoquinone, may help reduce inflammation and stress responses in the body. The research aims to provide insights into whether this natural oil can be used effectively to improve mental and physical well-being by examining its effects on stress hormones like cortisol, mood, sleep quality, and other aspects of daily life. Participants in the study take one capsule of either black seed oil or a placebo daily with a meal. The study evaluates their stress levels, mood, sleep, skin health, and focus, using various surveys and checks at four different times over two months. Saliva samples collected at home help measure cortisol, a stress hormone, to assess how it changes throughout the day. This method ensures researchers can accurately track changes in stress and related factors, aiming to determine if black seed oil can serve as a helpful tool for managing stress and enhancing quality of life.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.40 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Supportive Care Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.From 18 to 80 Years
Range of ages for which participants are eligible to join.Healthy volunteers allowed
If individuals who are healthy and do not have the condition being studied can participate.Criteria
Inclusion Criteria: * • Healthy moderately-stressed adults; Female and Male / Age 18-70 * Informed consent * Ability/desire to participate in 8-week supplement program Exclusion Criteria: * Inability to complete prescribed supplement regimen * Current use of incompatible medications or supplements, including anti-inflammatory or antidepressant medications and supplements in the last 4 weeks before the study and during the study * Auto-immune or inflammatory disease diagnosis * Pregnancy
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
50% chance of being blinded to the placebo group
Treatment Groups
Group I
PlaceboGroup II
ExperimentalStudy Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location