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CBD Oil for Reducing Emotional Impact of COVID-19 (CBDOIL)

Primary Purpose

Anxiety Depression, Alcohol Abuse, Substance Abuse

Status
Recruiting
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
CBD Isolate
Full Spectrum CBD Oil
Broad-Spectrum CBD Oil
Placebo Oil
Sponsored by
University of Texas at Austin
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Anxiety Depression focused on measuring CBD Oil, CBD Isolate, COVID-19, stress symptoms, RCT

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

INCLUSION CRITERIA:

  • Displays elevated symptom scores on one or more of the following established assessment instruments for depression (PROMIS-Depression), anxiety (PROMIS-Anxiety), Anger (PROMIS-Anger), sleep disturbance (PROMIS-Sleep); or Alcohol/Substance (PROMIS-Alcohol; PROMIS- Substance Use)
  • Age between 18 to 70;
  • Fluent in English;
  • Has home access to the Internet;
  • Willingness to provide signed informed consent;
  • Willingness to refrain from all non-study CBD products during the 6-week study period;
  • Willing to complete a brief pre-study 7-day online symptom monitoring log;

EXCLUSION CRITERIA:

  • History of a suicide attempt in the past 6 months;
  • Current medical problems that would preclude participating in the study including liver disease, current use of blood thinners, seizure medications, thyroid medications, or heart rhythm medications;
  • Pregnant or plan to become pregnant within the next 6 weeks;
  • Hx of adverse reactions to CBD oil or other CBD products;
  • Allergic to coconut oil.

Sites / Locations

  • University of Texas at Austin, Laboratory for the Study of Anxiety DisordersRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Active Comparator

Active Comparator

Active Comparator

Placebo Comparator

Arm Label

CBD-Isolate 300 mg.

Full-Spectrum CBD Oil 300 mg.

Broad-Spectrum CBD oil 300 mg.

Placebo Oil

Arm Description

Nightly oral administration of 300 mg. of CBD-Isolate for 28 consecutive days

Nightly oral administration of 300 mg. of Full Spectrum CBD Oil for 28 consecutive days

Nightly oral administration of 300 mg. of Broad-Spectrum CBD Oil for 28 consecutive days

Nightly oral administration of 300 mg. of Placebo Oil for 28 consecutive days

Outcomes

Primary Outcome Measures

PROMIS Emotional Distress Index
This measure is a 43-item patient-rated emotional distress symptom scale consisting of 6 sub-factors (Depression, Anxiety, Anger, Alcohol Use, Substance Use, and Sleep Disturbance). Each symptom is rated over a 7-day period on a 5-point scale.
PROMIS Emotional Distress Index
This measure is a 43-item patient-rated emotional distress symptom scale consisting of 6 sub-factors (Depression, Anxiety, Anger, Alcohol Use, Substance Use, and Sleep Disturbance). Each symptom is rated over a 7-day period on a 5-point scale.
PROMIS Emotional Distress Index
This measure is a 43-item patient-rated emotional distress symptom scale consisting of 6 sub-factors (Depression, Anxiety, Anger, Alcohol Use, Substance Use, and Sleep Disturbance). Each symptom is rated over a 7-day period on a 5-point scale.
PROMIS Emotional Distress Index
This measure is a 43-item patient-rated emotional distress symptom scale consisting of 6 sub-factors (Depression, Anxiety, Anger, Alcohol Use, Substance Use, and Sleep Disturbance). Each symptom is rated over a 7-day period on a 5-point scale.
PROMIS Emotional Distress Index
This measure is a 43-item patient-rated emotional distress symptom scale consisting of 6 sub-factors (Depression, Anxiety, Anger, Alcohol Use, Substance Use, and Sleep Disturbance). Each symptom is rated over a 7-day period on a 5-point scale.
PROMIS Emotional Distress Index
This measure is a 43-item patient-rated emotional distress symptom scale consisting of 6 sub-factors (Depression, Anxiety, Anger, Alcohol Use, Substance Use, and Sleep Disturbance). Each symptom is rated over a 7-day period on a 5-point scale.

Secondary Outcome Measures

PROMIS Depression Scale
This measure is an 8-item patient-rated depression symptom scale. Each symptom is rated over a 7-day period on a 5-point scale ranging from 1 (Never) to 5 (Always).
PROMIS Depression Scale
This measure is an 8-item patient-rated depression symptom scale. Each symptom is rated over a 7-day period on a 5-point scale ranging from 1 (Never) to 5 (Always).
PROMIS Depression Scale
This measure is an 8-item patient-rated depression symptom scale. Each symptom is rated over a 7-day period on a 5-point scale ranging from 1 (Never) to 5 (Always).
PROMIS Depression Scale
This measure is an 8-item patient-rated depression symptom scale. Each symptom is rated over a 7-day period on a 5-point scale ranging from 1 (Never) to 5 (Always).
PROMIS Depression Scale
This measure is an 8-item patient-rated depression symptom scale. Each symptom is rated over a 7-day period on a 5-point scale ranging from 1 (Never) to 5 (Always).
PROMIS Depression Scale
This measure is an 8-item patient-rated depression symptom scale. Each symptom is rated over a 7-day period on a 5-point scale ranging from 1 (Never) to 5 (Always).
PROMIS Anxiety Scale
This measure is an 8-item patient-rated anxiety symptom scale. Each symptom is rated over a 7-day period on a 5-point scale ranging from 1 (Never) to 5 (Always).
PROMIS Anxiety Scale
This measure is an 8-item patient-rated anxiety symptom scale. Each symptom is rated over a 7-day period on a 5-point scale ranging from 1 (Never) to 5 (Always).
PROMIS Anxiety Scale
This measure is an 8-item patient-rated anxiety symptom scale. Each symptom is rated over a 7-day period on a 5-point scale ranging from 1 (Never) to 5 (Always).
PROMIS Anxiety Scale
This measure is a 7-item patient-rated anxiety symptom scale. Each symptom is rated over a 7-day period on a 5-point scale ranging from 1 (Never) to 5 (Always).
PROMIS Anxiety Scale
This measure is a 7-item patient-rated anxiety symptom scale. Each symptom is rated over a 7-day period on a 5-point scale ranging from 1 (Never) to 5 (Always).
PROMIS Anxiety Scale
This measure is a 7-item patient-rated anxiety symptom scale. Each symptom is rated over a 7-day period on a 5-point scale ranging from 1 (Never) to 5 (Always).
PROMIS Anger Scale
This measure is a 5-item patient-rated anger symptom scale. Each symptom is rated over a 7-day period on a 5-point scale ranging from 1 (Never) to 5 (Always).
PROMIS Anger Scale
This measure is a 5-item patient-rated anger symptom scale. Each symptom is rated over a 7-day period on a 5-point scale ranging from 1 (Never) to 5 (Always).
PROMIS Anger Scale
This measure is a 5-item patient-rated anger symptom scale. Each symptom is rated over a 7-day period on a 5-point scale ranging from 1 (Never) to 5 (Always).
PROMIS Anger Scale
This measure is a 5-item patient-rated anger symptom scale. Each symptom is rated over a 7-day period on a 5-point scale ranging from 1 (Never) to 5 (Always).
PROMIS Anger Scale
This measure is a 5-item patient-rated anger symptom scale. Each symptom is rated over a 7-day period on a 5-point scale ranging from 1 (Never) to 5 (Always).
PROMIS Anger Scale
This measure is a 5-item patient-rated anger symptom scale. Each symptom is rated over a 7-day period on a 5-point scale ranging from 1 (Never) to 5 (Always).
PROMIS Alcohol Negative Consequences Scale
This measure is a 7-item patient-rated index of alcohol-related problems. Each item is rated over a 7-day period on a 5-point scale ranging from 1 (Never) to 5 (Always).
PROMIS Alcohol Negative Consequences Scale
This measure is a 7-item patient-rated index of alcohol-related problems. Each item is rated over a 7-day period on a 5-point scale ranging from 1 (Never) to 5 (Always).
PROMIS Alcohol Negative Consequences Scale
This measure is a 7-item patient-rated index of alcohol-related problems. Each item is rated over a 7-day period on a 5-point scale ranging from 1 (Never) to 5 (Always).
PROMIS Alcohol Negative Consequences Scale
This measure is a 7-item patient-rated index of alcohol-related problems. Each item is rated over a 7-day period on a 5-point scale ranging from 1 (Never) to 5 (Always).
PROMIS Alcohol Negative Consequences Scale
This measure is a 7-item patient-rated index of alcohol-related problems. Each item is rated over a 7-day period on a 5-point scale ranging from 1 (Never) to 5 (Always).
PROMIS Alcohol Negative Consequences Scale
This measure is a 7-item patient-rated index of alcohol-related problems. Each item is rated over a 7-day period on a 5-point scale ranging from 1 (Never) to 5 (Always).
PROMIS Sleep Disturbance Scale
This measure is an 8-item patient-rated index of sleep disturbance. Each item is rated over a 7-day period on a 5-point scale ranging from 1 (Not at all) to 5 (Very Much).
PROMIS Sleep Disturbance Scale
This measure is an 8-item patient-rated index of sleep disturbance. Each item is rated over a 7-day period on a 5-point scale ranging from 1 (Not at all) to 5 (Very Much).
PROMIS Sleep Disturbance Scale
This measure is an 8-item patient-rated index of sleep disturbance. Each item is rated over a 7-day period on a 5-point scale ranging from 1 (Not at all) to 5 (Very Much).
PROMIS Sleep Disturbance Scale
This measure is an 8-item patient-rated index of sleep disturbance. Each item is rated over a 7-day period on a 5-point scale ranging from 1 (Not at all) to 5 (Very Much).
PROMIS Sleep Disturbance Scale
This measure is an 8-item patient-rated index of sleep disturbance. Each item is rated over a 7-day period on a 5-point scale ranging from 1 (Not at all) to 5 (Very Much).
PROMIS Sleep Disturbance Scale
This measure is an 8-item patient-rated index of sleep disturbance. Each item is rated over a 7-day period on a 5-point scale ranging from 1 (Not at all) to 5 (Very Much).
COVID-19 Coping Self-Efficacy
This measure is a 15-item author-constructed patient-rated index of COVID-19 Coping Self-Efficacy
COVID-19 Coping Self-Efficacy
This measure is a 15-item author-constructed patient-rated index of COVID-19 Coping Self-Efficacy
COVID-19 Coping Self-Efficacy
This measure is a 15-item author-constructed patient-rated index of COVID-19 Coping Self-Efficacy
COVID-19 Coping Self-Efficacy
This measure is a 15-item author-constructed patient-rated index of COVID-19 Coping Self-Efficacy
COVID-19 Coping Self-Efficacy
This measure is a 15-item author-constructed patient-rated index of COVID-19 Coping Self-Efficacy
COVID-19 Coping Self-Efficacy
This measure is a 15-item author-constructed patient-rated index of COVID-19 Coping Self-Efficacy
Sheehan Disability Scale
This measure is a 3-item patient-rated index of level of functional impairment.
Sheehan Disability Scale
This measure is a 3-item patient-rated index of level of functional impairment.

Full Information

First Posted
October 3, 2020
Last Updated
July 7, 2023
Sponsor
University of Texas at Austin
Collaborators
Way West Wellness, SunFlora.Inc
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1. Study Identification

Unique Protocol Identification Number
NCT04603781
Brief Title
CBD Oil for Reducing Emotional Impact of COVID-19
Acronym
CBDOIL
Official Title
Use of CBD Oil for Reducing the Negative Emotional Impact of COVID-19: A Randomized Placebo-Controlled Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Recruiting
Study Start Date
December 4, 2020 (Actual)
Primary Completion Date
December 31, 2023 (Anticipated)
Study Completion Date
December 31, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Texas at Austin
Collaborators
Way West Wellness, SunFlora.Inc

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Our purpose is to conduct a 4-arm placebo-controlled clinical trial to investigate the relative clinical efficacy of 300 mg. of pure hemp-derived CBD isolate, 300 mg. of full spectrum CBD oil, 300 mg. of broad- spectrum CBD Oil, or Placebo oil among adults presenting with COVID-19 -induced stress reactions including one or more of the following: anxiety, depression, anger, substance use, or sleep disturbance.
Detailed Description
Background and Significance of the Proposed Project The COVID-19 pandemic has hit us like a ton of bricks creating unimaginable levels of unanticipated death, financial hardship, and dramatic changes in nearly every facet of our life including school, work, shopping, social and family life. Sadly, the physical, mental, economic, and health burden of COVID-19 disproportionately affects the poor, the elderly, and people of color. The stress induced by these changes as well as the lack of control we have over them increases risk for new onset of mental health problems such as anxiety, depression, substance abuse, sleep disturbance, and family violence as well as exacerbation of symptoms among those with pre-existing psychiatric conditions. Although many people will successfully manage the increased stress from COVID-19 on their own or with the support from family and friends, others may need extra help to cope. Consequently, there is an urgent need for developing cost-effective strategies for managing the stress-induced psychological consequences of COVID-19. There's been considerable excitement in the press over the potential therapeutic use of cannabidiol (CBD) products in the treatment of a variety of physical and mental health problems. Delta-9-tetrahydrocannabinol (delta-9 THC) is still illegal in most states because of its psychoactive abuse potential. In contrast, cannabidiol (CBD) does not convert to THC in the body and has negligible side effects relative to main-stream psychiatric drugs (benzodiazepines and antidepressants) commonly prescribed for the treatment of stress-related disorders such as anxiety, depression, and insomnia. Mounting evidence from studies with rodents suggests that CBD may confer significant promising health-related benefits including anti-inflammatory, pain-relieving, anti-cancer, memory enhancement, and facilitation of fear extinction (see White for a recent review). The biggest success story for CBD use in humans to date comes from placebo-controlled randomized clinical trials demonstrating a 50% or more reduction in previously intractable seizures in children suffering from Dravet syndrome and Lennox-Gastaut syndrome. Moreover, several controlled clinical trials have shown promising findings in reducing psychotic symptoms among patients with schizophrenia and among young adults displaying THC-induced psychosis. Preliminary Evidence that CBD may offer promise in the treatment of stress-related disorders has started to emerge. A small pilot trial with 24 patients presenting with social anxiety disorder found that relative to placebo, a single dose of 100 mg of CBD oil led to lower levels of anxiety, cognitive impairment, and discomfort in their actual speech performance as well as their anxiety before the speech. An uncontrolled case series of 11 PTSD patients receiving 8 weeks of CBD, reported a 28% reduction in PTSD symptom scores. In a small 4-week placebo-controlled study of 37 young Japanese adults with social anxiety disorder, Masataka found a significant advantage of CBD over placebo in reducing subjects' scores on two widely used measures of social anxiety symptoms. Why Compare CBD-Isolate with Broad-Spectrum and Full-Spectrum CBD? CBD isolate is the purest form of CBD. It is made by extracting it from its natural environment - either hemp which is legal and recognized as generally safe in all states because of its low THC content (less than .3%), or the marijuana plant which has high levels of THC (up to 30%) and remains a Schedule 1 controlled substance under the Controlled Substances Act of 1970. Unlike hemp-derived CBD Isolate, hemp-derived full-spectrum CBD contains all the hundreds of phytochemicals naturally found in the cannabis plant, including CBD, trace cannabinoids including Cannabinol (CBN), Cannabichromene (CBC), Cannabigerol (CBDA) and Cannabidivarin (CBDV), and more than 200 different terpenes, essential oils, and negligible THC content (less than 0.3%). Research demonstrating the wide-ranging therapeutic effects of CBD oil including anti-emetic, anti-inflammatory, anxiolytic, and anti-psychotic effects were based on studies using pure doses of CBD Isolate. However, more recently it has been shown that the therapeutic effects of purified CBD display a bell-shaped dose-response curve suggesting a limited dose range, with no beneficial effects achieved at either lower or higher doses. This narrow therapeutic window presents a challenge for using CBD isolate clinically. Based on recent research with rodents and humans, administration of a full spectrum cannabis extract containing mostly CBD but also containing other minor phytocannabinoids and non-cannabinoids exerted a synergistic effect with CBD that was both more effective than CBD Isolate without the unwanted bell-shaped dose-response curve. This finding has been named the entourage effect. However, to date, there are no human trials for any physical or mental health problem comparing the gold standard CBD isolate with a full-spectrum CBD formulation, despite the fact that both forms of CBD are widely available without a prescription in stores all across the United States. The proposed project will provide important data to determine whether a full-spectrum CBD formulation offers any advantages over CBD isolate in reducing COVID-19 stress-induced symptoms. Specific Aims and Hypotheses: Compare the efficacy of a 4-week daily regimen of hemp-derived CBD isolate (300 mg/day), broad-spectrum CBD oil, full spectrum CBD oil (300 mg/day), or placebo oil in reducing patient-rated symptoms of stress, anxiety, depression, and sleep disturbance. It is predicted that patients receiving and of the three active CBD oil formulations (pure isolate, broad-spectrum, or full spectrum CBD oil) will show significantly greater reduction in emotional distress and sleep disturbance relative to those receiving placebo oil. It is also predicted that broad-spectrum and full-spectrum CBD oil will outperform CBD isolate in reducing COVID-19 stress-induced symptoms of stress, anxiety, depression, anger, and sleep disturbance. Examine predictors of patients' clinical response to the 4 treatments. It is expected that the superiority of broad-spectrum and full-spectrum CBD oil relative to CBD isolate or placebo will be more pronounced for patients showing more severe COVID-19 stress-induced symptoms at baseline. Examine the perceived acceptability and side effects profile of 4 weeks of daily CBD/Placebo oil ingestion. It is expected that each of the three CBD formulations (CBD isolate, Broad-spectrum or Full spectrum CBD oil) will show minimal side effects that will not exceed the level of side effects for those ingesting placebo oil with the possible exception of somnolence.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Anxiety Depression, Alcohol Abuse, Substance Abuse, Anger, Sleep Disturbance, Stress Reaction
Keywords
CBD Oil, CBD Isolate, COVID-19, stress symptoms, RCT

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Model Description
4-arm double-blind placebo-controlled trial
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Masking Description
The PI and all members of the study team will be blind to the drug assignment of the patient. Only the CBD suppliers (John Fornecker- Way West and Anthony Ferrari - SunMed CBD) and a UT LSAD staff member (not connected to the study) will have access to participants' treatment assignment. In the very unlikely event that a participant should have an adverse reaction requiring medical attention, the PI will contact the UT staff person who is keeper of the blind and request the treatment assignment of the subject in question without revealing the treatment condition coding scheme.
Allocation
Randomized
Enrollment
200 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
CBD-Isolate 300 mg.
Arm Type
Active Comparator
Arm Description
Nightly oral administration of 300 mg. of CBD-Isolate for 28 consecutive days
Arm Title
Full-Spectrum CBD Oil 300 mg.
Arm Type
Active Comparator
Arm Description
Nightly oral administration of 300 mg. of Full Spectrum CBD Oil for 28 consecutive days
Arm Title
Broad-Spectrum CBD oil 300 mg.
Arm Type
Active Comparator
Arm Description
Nightly oral administration of 300 mg. of Broad-Spectrum CBD Oil for 28 consecutive days
Arm Title
Placebo Oil
Arm Type
Placebo Comparator
Arm Description
Nightly oral administration of 300 mg. of Placebo Oil for 28 consecutive days
Intervention Type
Dietary Supplement
Intervention Name(s)
CBD Isolate
Other Intervention Name(s)
Pure CBD oil
Intervention Description
300 mg. daily dose of CBD Isolate Oil
Intervention Type
Dietary Supplement
Intervention Name(s)
Full Spectrum CBD Oil
Intervention Description
300 mg. daily dose of CBD with full spectrum of other cannabinoids found in the hemp plant
Intervention Type
Dietary Supplement
Intervention Name(s)
Broad-Spectrum CBD Oil
Intervention Description
300 mg. daily dose of CBD with a selected spectrum of other cannabinoids found in the hemp plant
Intervention Type
Dietary Supplement
Intervention Name(s)
Placebo Oil
Intervention Description
MCT Oil with mint flavoring
Primary Outcome Measure Information:
Title
PROMIS Emotional Distress Index
Description
This measure is a 43-item patient-rated emotional distress symptom scale consisting of 6 sub-factors (Depression, Anxiety, Anger, Alcohol Use, Substance Use, and Sleep Disturbance). Each symptom is rated over a 7-day period on a 5-point scale.
Time Frame
Week 0-Baseline
Title
PROMIS Emotional Distress Index
Description
This measure is a 43-item patient-rated emotional distress symptom scale consisting of 6 sub-factors (Depression, Anxiety, Anger, Alcohol Use, Substance Use, and Sleep Disturbance). Each symptom is rated over a 7-day period on a 5-point scale.
Time Frame
Week 1-Treatment
Title
PROMIS Emotional Distress Index
Description
This measure is a 43-item patient-rated emotional distress symptom scale consisting of 6 sub-factors (Depression, Anxiety, Anger, Alcohol Use, Substance Use, and Sleep Disturbance). Each symptom is rated over a 7-day period on a 5-point scale.
Time Frame
Week 2-Treatment
Title
PROMIS Emotional Distress Index
Description
This measure is a 43-item patient-rated emotional distress symptom scale consisting of 6 sub-factors (Depression, Anxiety, Anger, Alcohol Use, Substance Use, and Sleep Disturbance). Each symptom is rated over a 7-day period on a 5-point scale.
Time Frame
Week 3-Treatment
Title
PROMIS Emotional Distress Index
Description
This measure is a 43-item patient-rated emotional distress symptom scale consisting of 6 sub-factors (Depression, Anxiety, Anger, Alcohol Use, Substance Use, and Sleep Disturbance). Each symptom is rated over a 7-day period on a 5-point scale.
Time Frame
Week 4-Treatment
Title
PROMIS Emotional Distress Index
Description
This measure is a 43-item patient-rated emotional distress symptom scale consisting of 6 sub-factors (Depression, Anxiety, Anger, Alcohol Use, Substance Use, and Sleep Disturbance). Each symptom is rated over a 7-day period on a 5-point scale.
Time Frame
Week 5-Follow-up
Secondary Outcome Measure Information:
Title
PROMIS Depression Scale
Description
This measure is an 8-item patient-rated depression symptom scale. Each symptom is rated over a 7-day period on a 5-point scale ranging from 1 (Never) to 5 (Always).
Time Frame
Week 0-Baseline
Title
PROMIS Depression Scale
Description
This measure is an 8-item patient-rated depression symptom scale. Each symptom is rated over a 7-day period on a 5-point scale ranging from 1 (Never) to 5 (Always).
Time Frame
Week 1-Treatment
Title
PROMIS Depression Scale
Description
This measure is an 8-item patient-rated depression symptom scale. Each symptom is rated over a 7-day period on a 5-point scale ranging from 1 (Never) to 5 (Always).
Time Frame
Week 2-Treatment
Title
PROMIS Depression Scale
Description
This measure is an 8-item patient-rated depression symptom scale. Each symptom is rated over a 7-day period on a 5-point scale ranging from 1 (Never) to 5 (Always).
Time Frame
Week 3-Treatment
Title
PROMIS Depression Scale
Description
This measure is an 8-item patient-rated depression symptom scale. Each symptom is rated over a 7-day period on a 5-point scale ranging from 1 (Never) to 5 (Always).
Time Frame
Week 4-Treatment
Title
PROMIS Depression Scale
Description
This measure is an 8-item patient-rated depression symptom scale. Each symptom is rated over a 7-day period on a 5-point scale ranging from 1 (Never) to 5 (Always).
Time Frame
Week 5-Follow-up
Title
PROMIS Anxiety Scale
Description
This measure is an 8-item patient-rated anxiety symptom scale. Each symptom is rated over a 7-day period on a 5-point scale ranging from 1 (Never) to 5 (Always).
Time Frame
Week 0- Baseline
Title
PROMIS Anxiety Scale
Description
This measure is an 8-item patient-rated anxiety symptom scale. Each symptom is rated over a 7-day period on a 5-point scale ranging from 1 (Never) to 5 (Always).
Time Frame
Week 1-Treatment
Title
PROMIS Anxiety Scale
Description
This measure is an 8-item patient-rated anxiety symptom scale. Each symptom is rated over a 7-day period on a 5-point scale ranging from 1 (Never) to 5 (Always).
Time Frame
Week 2-Treatment
Title
PROMIS Anxiety Scale
Description
This measure is a 7-item patient-rated anxiety symptom scale. Each symptom is rated over a 7-day period on a 5-point scale ranging from 1 (Never) to 5 (Always).
Time Frame
Week 3-Treatment
Title
PROMIS Anxiety Scale
Description
This measure is a 7-item patient-rated anxiety symptom scale. Each symptom is rated over a 7-day period on a 5-point scale ranging from 1 (Never) to 5 (Always).
Time Frame
Week 4-Treatment
Title
PROMIS Anxiety Scale
Description
This measure is a 7-item patient-rated anxiety symptom scale. Each symptom is rated over a 7-day period on a 5-point scale ranging from 1 (Never) to 5 (Always).
Time Frame
Week 5-Follow-up
Title
PROMIS Anger Scale
Description
This measure is a 5-item patient-rated anger symptom scale. Each symptom is rated over a 7-day period on a 5-point scale ranging from 1 (Never) to 5 (Always).
Time Frame
Week 0- Baseline
Title
PROMIS Anger Scale
Description
This measure is a 5-item patient-rated anger symptom scale. Each symptom is rated over a 7-day period on a 5-point scale ranging from 1 (Never) to 5 (Always).
Time Frame
Week 1- Treatment
Title
PROMIS Anger Scale
Description
This measure is a 5-item patient-rated anger symptom scale. Each symptom is rated over a 7-day period on a 5-point scale ranging from 1 (Never) to 5 (Always).
Time Frame
Week 2- Treatment
Title
PROMIS Anger Scale
Description
This measure is a 5-item patient-rated anger symptom scale. Each symptom is rated over a 7-day period on a 5-point scale ranging from 1 (Never) to 5 (Always).
Time Frame
Week 3- Treatment
Title
PROMIS Anger Scale
Description
This measure is a 5-item patient-rated anger symptom scale. Each symptom is rated over a 7-day period on a 5-point scale ranging from 1 (Never) to 5 (Always).
Time Frame
Week 4- Treatment
Title
PROMIS Anger Scale
Description
This measure is a 5-item patient-rated anger symptom scale. Each symptom is rated over a 7-day period on a 5-point scale ranging from 1 (Never) to 5 (Always).
Time Frame
Week 5- Follow-up
Title
PROMIS Alcohol Negative Consequences Scale
Description
This measure is a 7-item patient-rated index of alcohol-related problems. Each item is rated over a 7-day period on a 5-point scale ranging from 1 (Never) to 5 (Always).
Time Frame
Week 0- Baseline
Title
PROMIS Alcohol Negative Consequences Scale
Description
This measure is a 7-item patient-rated index of alcohol-related problems. Each item is rated over a 7-day period on a 5-point scale ranging from 1 (Never) to 5 (Always).
Time Frame
Week 1- Treatment
Title
PROMIS Alcohol Negative Consequences Scale
Description
This measure is a 7-item patient-rated index of alcohol-related problems. Each item is rated over a 7-day period on a 5-point scale ranging from 1 (Never) to 5 (Always).
Time Frame
Week 2- Treatment
Title
PROMIS Alcohol Negative Consequences Scale
Description
This measure is a 7-item patient-rated index of alcohol-related problems. Each item is rated over a 7-day period on a 5-point scale ranging from 1 (Never) to 5 (Always).
Time Frame
Week 3- Treatment
Title
PROMIS Alcohol Negative Consequences Scale
Description
This measure is a 7-item patient-rated index of alcohol-related problems. Each item is rated over a 7-day period on a 5-point scale ranging from 1 (Never) to 5 (Always).
Time Frame
Week 4- Treatment
Title
PROMIS Alcohol Negative Consequences Scale
Description
This measure is a 7-item patient-rated index of alcohol-related problems. Each item is rated over a 7-day period on a 5-point scale ranging from 1 (Never) to 5 (Always).
Time Frame
Week 5- Follow-up
Title
PROMIS Sleep Disturbance Scale
Description
This measure is an 8-item patient-rated index of sleep disturbance. Each item is rated over a 7-day period on a 5-point scale ranging from 1 (Not at all) to 5 (Very Much).
Time Frame
Week 0- Baseline
Title
PROMIS Sleep Disturbance Scale
Description
This measure is an 8-item patient-rated index of sleep disturbance. Each item is rated over a 7-day period on a 5-point scale ranging from 1 (Not at all) to 5 (Very Much).
Time Frame
Week 1- Treatment
Title
PROMIS Sleep Disturbance Scale
Description
This measure is an 8-item patient-rated index of sleep disturbance. Each item is rated over a 7-day period on a 5-point scale ranging from 1 (Not at all) to 5 (Very Much).
Time Frame
Week 2- Treatment
Title
PROMIS Sleep Disturbance Scale
Description
This measure is an 8-item patient-rated index of sleep disturbance. Each item is rated over a 7-day period on a 5-point scale ranging from 1 (Not at all) to 5 (Very Much).
Time Frame
Week 3- Treatment
Title
PROMIS Sleep Disturbance Scale
Description
This measure is an 8-item patient-rated index of sleep disturbance. Each item is rated over a 7-day period on a 5-point scale ranging from 1 (Not at all) to 5 (Very Much).
Time Frame
Week 4- Treatment
Title
PROMIS Sleep Disturbance Scale
Description
This measure is an 8-item patient-rated index of sleep disturbance. Each item is rated over a 7-day period on a 5-point scale ranging from 1 (Not at all) to 5 (Very Much).
Time Frame
Week 5- Follow-up
Title
COVID-19 Coping Self-Efficacy
Description
This measure is a 15-item author-constructed patient-rated index of COVID-19 Coping Self-Efficacy
Time Frame
Week 0- Baseline
Title
COVID-19 Coping Self-Efficacy
Description
This measure is a 15-item author-constructed patient-rated index of COVID-19 Coping Self-Efficacy
Time Frame
Week 1- Treatment
Title
COVID-19 Coping Self-Efficacy
Description
This measure is a 15-item author-constructed patient-rated index of COVID-19 Coping Self-Efficacy
Time Frame
Week 2- Treatment
Title
COVID-19 Coping Self-Efficacy
Description
This measure is a 15-item author-constructed patient-rated index of COVID-19 Coping Self-Efficacy
Time Frame
Week 3- Treatment
Title
COVID-19 Coping Self-Efficacy
Description
This measure is a 15-item author-constructed patient-rated index of COVID-19 Coping Self-Efficacy
Time Frame
Week 4- Treatment
Title
COVID-19 Coping Self-Efficacy
Description
This measure is a 15-item author-constructed patient-rated index of COVID-19 Coping Self-Efficacy
Time Frame
Week 5- Follow-up
Title
Sheehan Disability Scale
Description
This measure is a 3-item patient-rated index of level of functional impairment.
Time Frame
Week 0- Baseline
Title
Sheehan Disability Scale
Description
This measure is a 3-item patient-rated index of level of functional impairment.
Time Frame
Week 5- Follow-up

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
INCLUSION CRITERIA: Displays elevated symptom scores on one or more of the following established assessment instruments for depression (PROMIS-Depression), anxiety (PROMIS-Anxiety), Anger (PROMIS-Anger), sleep disturbance (PROMIS-Sleep); or Alcohol/Substance (PROMIS-Alcohol; PROMIS- Substance Use) Age between 18 to 70; Fluent in English; Has home access to the Internet; Willingness to provide signed informed consent; Willingness to refrain from all non-study CBD products during the 6-week study period; Willing to complete a brief pre-study 7-day online symptom monitoring log; Currently residing in the United States EXCLUSION CRITERIA: History of a suicide attempt within the past 6 months Any medical problem that would preclude participating in the study including liver disease Current use of warfarin or other prescribed blood thinners, Currently taking seizure medications such as valproate, lamotrigine, or clobazam; Currently taking thyroid medications such as levothyroxine; Currently taking heart rhythm medications such as amiodarone; Currently taking anti-hypertension medications; Pregnant or planning to become pregnant within the next 6 weeks. History of adverse reaction to CBD oil or other CBD products. Allergic to coconut oil.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Michael J Telch, Ph.D.
Phone
(512) 814-5480
Email
Telch@austin.utexas.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Cate Fischer, M.A.
Phone
(512) 522-6216
Email
utcbdstudy@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michael J Telch, Ph.D.
Organizational Affiliation
University of Texas at Austin
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Texas at Austin, Laboratory for the Study of Anxiety Disorders
City
Austin
State/Province
Texas
ZIP/Postal Code
78712
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Michael J Telch, Ph.D.
Phone
512-814-5480
Email
Telch@austin.utexas.edu
First Name & Middle Initial & Last Name & Degree
Cate Fischer, MA
Phone
(512) 522-6216
Email
utcbdstudy@gmail.com
First Name & Middle Initial & Last Name & Degree
Michael J Telch, Ph.D.

12. IPD Sharing Statement

Plan to Share IPD
No
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CBD Oil for Reducing Emotional Impact of COVID-19

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