- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04026672
Hemp Oil + User Experience Study
February 6, 2020 updated by: Thorne Research Inc.
Hemp Oil + User Experience Study: A Retrospective, Non-Interventional Study to Assess Consumer Experience and the Impact of Hemp Oil + on Quality of Life
Presented as an online survey, this study seeks to better understand how Thorne customers are using and experiencing the new Hemp Oil + product and how they feel it compares in the marketplace.
Hemp Oil + is a combination product with a proprietary blend of hemp, clove, black pepper, hops, and rosemary extracts.
People who have independently elected to purchase and use Hemp Oil + before the study starts will be invited to voluntarily participate.
If they meet study requirements and give consent they will answer questions online about their experience with Hemp Oil +.
Questions address general demographics and wellness, general impressions of the product, how it compares to other products, and any effect it has had on their gastrointestinal health, physical discomfort, sleep, and mood.
The survey is expected to take 15-30 min of participant time.
Data will be analyzed to determine whether the customer experience with Hemp Oil + is as favorable as it seems from anecdotal reports.
Analysis will also be conducted to find patterns that can inform future studies, marketing, and customer education efforts.
Study Overview
Status
Completed
Study Type
Observational
Enrollment (Actual)
201
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
South Carolina
-
Summerville, South Carolina, United States, 29486
- Online Survey for Thorne Research, Inc.
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
N/A
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
People who have purchased Hemp Oil +
Description
Inclusion Criteria:
- Has personally used at least one bottle (30 gelcaps) of Hemp Oil +
- Provides consent to participate in the study
Exclusion Criteria:
- Cannot access or use the electronic survey for any reason
- Was pregnant or nursing when taking Hemp Oil +
- Is a Thorne employee not willing to participate without compensation
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Assess impact to overall quality of life (QoL) after taking Hemp Oil +
Time Frame: 1 Day
|
Questionnaire gathering data from the past 30 or more days
|
1 Day
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Assess impact to specific QoL factors - GI health, mood, sleep, physical discomfort - after taking Hemp Oil +
Time Frame: 1 Day
|
Questionnaire gathering data from the past 30 or more days
|
1 Day
|
|
Gain insight into user perspective on product quality, efficacy, and rationale for continuing/discontinuing use
Time Frame: 1 Day
|
Questionnaire gathering data from the past 30 or more days
|
1 Day
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Jacqueline Jacques, ND, Thorne Research
- Principal Investigator: Sheena Smith, MS, Thorne Research
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 22, 2020
Primary Completion (Actual)
February 4, 2020
Study Completion (Actual)
February 4, 2020
Study Registration Dates
First Submitted
June 28, 2019
First Submitted That Met QC Criteria
July 17, 2019
First Posted (Actual)
July 19, 2019
Study Record Updates
Last Update Posted (Actual)
February 10, 2020
Last Update Submitted That Met QC Criteria
February 6, 2020
Last Verified
February 1, 2020
More Information
Terms related to this study
Other Study ID Numbers
- Hemp-PM001
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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