- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04507087
Documentary to Encourage Plant-based Eating
March 15, 2021 updated by: Maya Mathur, Stanford University
Randomized Controlled Trial of a Documentary to Encourage Plant-based Eating
This study will assess whether watching a documentary video about the health, environmental, and ethical consequences of eating meat and animal products reduces participants' self-reported intake of these items.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
See detailed preregistration: https://osf.io/xrckh/registrations
Study Type
Interventional
Enrollment (Actual)
650
Phase
- Not Applicable
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
-
-
California
-
Palo Alto, California, United States, 94304
- Maya Mathur
-
-
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
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Participant is currently located in the United States
- Participant is at least 18 years old
Exclusion Criteria:
- Participant is located outside the United States
- Participant is less than 18 years old
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
- Primary Purpose: OTHER
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
EXPERIMENTAL: Intervention
See detailed preregistration: https://osf.io/xrckh/registrations
|
A 20-minute documentary about the health, environmental, and animal welfare consequences of eating meat and animal products
|
SHAM_COMPARATOR: Control
See detailed preregistration: https://osf.io/xrckh/registrations
|
A 20-minute unrelated video (a motivational talk entitled "Listening to shame")
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Total meat and animal product consumption
Time Frame: Consumption over the 1-week time frame spanning approximately 1 week to 2 weeks after baseline data collection
|
Self-reported meat and animal product consumption (ounces consumed over the past week)
|
Consumption over the 1-week time frame spanning approximately 1 week to 2 weeks after baseline data collection
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Total meat consumption
Time Frame: Consumption over the 1-week time frame spanning approximately 1 week to 2 weeks after baseline data collection
|
Self-reported meat consumption (ounces consumed over the past week)
|
Consumption over the 1-week time frame spanning approximately 1 week to 2 weeks after baseline data collection
|
Total animal product consumption
Time Frame: Consumption over the 1-week time frame spanning approximately 1 week to 2 weeks after baseline data collection
|
Self-reported animal product consumption (ounces consumed over the past week)
|
Consumption over the 1-week time frame spanning approximately 1 week to 2 weeks after baseline data collection
|
Consumption of each of 8 individual categories of meats and animal products
Time Frame: Consumption over the 1-week time frame spanning approximately 1 week to 2 weeks after baseline data collection
|
Self-reported consumption (ounces consumed over the past week)
|
Consumption over the 1-week time frame spanning approximately 1 week to 2 weeks after baseline data collection
|
Total consumption of selected, healthy plant-based foods (ounces consumed over the past week)
Time Frame: Consumption over the 1-week time frame spanning approximately 1 week to 2 weeks after baseline data collection
|
Self-reported consumption (ounces consumed over the past week)
|
Consumption over the 1-week time frame spanning approximately 1 week to 2 weeks after baseline data collection
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Perceived importance of health
Time Frame: 2 weeks after baseline data collection
|
A single Likert item adapted from Heckler (2010), ranging from 1 to 6, with higher scores representing greater perceived importance.
The exact text is provided in detailed preregistration: https://osf.io/xrckh/registrations.
|
2 weeks after baseline data collection
|
Perceived importance of environmental sustainability
Time Frame: 2 weeks after baseline data collection
|
A single Likert item adapted from Heckler (2010), ranging from 1 to 6, with higher scores representing greater perceived importance.
The exact text is provided in detailed preregistration: https://osf.io/xrckh/registrations.
|
2 weeks after baseline data collection
|
Perceived importance of animal welfare
Time Frame: 2 weeks after baseline data collection
|
A single Likert item adapted from Heckler (2010), ranging from 1 to 6, with higher scores representing greater perceived importance.
The exact text is provided in detailed preregistration: https://osf.io/xrckh/registrations.
|
2 weeks after baseline data collection
|
Speciesism
Time Frame: 2 weeks after baseline data collection
|
Caviola et al.'s (2019) Speciesism Scale, consisting of 6 Likert items each ranging from 1 to 7. After reverse-coding, a higher score on the sum of the items (ranging from 6 to 42) represents greater speciesism.
The exact text for all items is provided in detailed preregistration: https://osf.io/xrckh/registrations.
|
2 weeks after baseline data collection
|
Interest in animal welfare activism and reform
Time Frame: 2 weeks after baseline data collection
|
2 items modified from Corning et al.'s (2002) Activism Orientation Scale as well as 3 novel items, consisting in total of 5 items each ranging from 1 to 7. A higher score on the sum of the items (ranging from 5 to 35) represents greater interest in activism and reform.
The exact text for all items is provided in detailed preregistration: https://osf.io/xrckh/registrations.
|
2 weeks after baseline data collection
|
Social dominance orientation
Time Frame: 2 weeks after baseline data collection
|
Ho et al.'s (2015) 8-item Social Dominance Orientation [SDO(7)] scale, consisting in total of 5 items each ranging from 1 to 7. After reverse-coding, a higher score on the sum of the items (ranging from 8 to 56) represents greater interest in activism and reform.
The exact text for all items is provided in detailed preregistration: https://osf.io/xrckh/registrations.
|
2 weeks after baseline data collection
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Maya B Mathur, PhD, Stanford University
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
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)
August 26, 2020
Primary Completion (ACTUAL)
September 7, 2020
Study Completion (ACTUAL)
December 31, 2020
Study Registration Dates
First Submitted
July 31, 2020
First Submitted That Met QC Criteria
August 5, 2020
First Posted (ACTUAL)
August 11, 2020
Study Record Updates
Last Update Posted (ACTUAL)
March 17, 2021
Last Update Submitted That Met QC Criteria
March 15, 2021
Last Verified
March 1, 2021
More Information
Terms related to this study
Other Study ID Numbers
- eatingveg
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Plan Description
All materials and analysis code required to reproduce all results will be made publicly available.
All data except for participants' counties of residence (which is considered identifying information) will also be made publicly available.
IPD Sharing Time Frame
Immediately upon journal acceptance or earlier if possible given embargo policies.
IPD Sharing Access Criteria
Public availability
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
- ICF
- ANALYTIC_CODE
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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