- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04803448
Patient Doctor Lies
Patient Doctor Lies: When is Privacy Assurance a Bad Thing? A Randomized Clinical Trial
Accurate patient information disclosure is critical to provide optimal treatment. Methods that can detect and then increase the truthfulness of information are relatively unknown.
To investigate the impact of communication about privacy, benefits, and risk on patient truthfulness, the investigators test two new methods to detect patient truthfulness and demonstrate the effects of privacy notices (e.g. HIPPA statements).
Participants include a national online sample randomly assigned to one of six treatment statements that might be typically given before health information was requested. The assigned treatments include one or mix of the following: privacy notice, statement of the benefits of accurate disclosure, and statement of the risks of inaccurate disclosure and control of no statement before being asked typical health questions.
The investigators propose that based on elaboration likelihood model, statements reminding participants of their privacy will increase lying.
The investigators hypothesis the use of a new biometric mouse movement lie detection method and answer adjustment can measure patient lies.
The investigators hypothesis that reminders of the risk of not telling the truth will reduce lying due to risk aversion.
Lastly the investigators hypothesis that statements of benefits of answering truthfully will increase truthfulness.
Study Overview
Status
Conditions
Detailed Description
After agreeing to an IRB-approved modified consent form designed to hide the true purpose of the study to detect lying, all participants will complete the CESD-10 depression scale. This validated measure of depression was used in order to simulate the false pretense of the experiment.
This online survey randomly assigns participating adults to one of six intervention statements after which they are asked eight typical questions about their health. The statements include:
- control (no stimuli)
- benefit (statement about the benefits of accurate information disclosure)
- risk (statement about the risks of inaccurate information disclosure)
- privacy (a traditional medical privacy notification and seal image)
- privacy + benefit
- privacy + risk After this intervention participants are asked to disclose eight items of personal health information, including their weight, height, alcohol intake, illegal drug use, prescription drug abuse, smoking, exercise, and sexual activity. We do not assess these actual numbers. They will be the basis for assessing truthfulness by answer adjustment or biometric mouse-movement.
An example of an intervention benefit statement followed by a health question about weight reads: "What is your weight? Accurately answering this will increase the likelihood of a correct diagnosis." A risk statement reads: "What is your weight? Inaccurately answering this will increase the likelihood of an incorrect diagnosis." A privacy statement read: "What is your weight? We will not share or sell this personal health information with anyone. We will comply with all HIPPA regulations regarding the protection of your data."
The dependent variable - patient truthfulness, will be measured in two ways.
- First measure of truthfulness will be a biometric mouse-movement measure. As participants answer the health care questions coded programming will measure the mouse-movement arc distance and time to response for biometric lie detection. This measurement is completed when participants move to their response to each health question.
- Second measure of truthfulness will be the answer adjustment method. Participants will be given a summary of their answers from their health questions in a read-only format and asked to indicate how OVER of UNDERSTATED each initial response was (e.g., "You indicated that your current weight is 185 lbs. How overstated or understated is that value?") on a scale from -5 (understated) to 5 (overstated). The absolute value of their scaled response represents the extent to which participants' initial response deviated from the truth. This the unit of measure to be used in analysis.
- The answer adjustment values and the mouse tracking results provide a more holistic measure of truthfulness than one alone.
No personal identifiers are collected. Age and gender are collected.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Utah
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Provo, Utah, United States, 84602
- Brigham Young University
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Adults
- Individuals 18-80 years
- English speaking
- Live in the United States
Exclusion Criteria:
- Participants that do not complete the survey
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
No Intervention: Control
No statement is provided before asking the health care question.
Example: What is your weight in pounds?
|
|
Experimental: Benefit Statement
A statement of benefit will be given (see intervention) after the health question.
|
The participant reads this statement after asked one of eight health questions
An example of this with one of the 8 health questions is... What number of days in the last 2 weeks you engaged in >30 minutes of exercise? Accurately answering this will increase the likelihood of a correct diagnosis. |
Experimental: Risk Statement
A statement of risk will be given (see intervention) after the health question.
|
The participant reads this statement after being asked one of eight health questions. The statement reads: Inaccurately answering this will increase the likelihood of an incorrect diagnosis. |
Experimental: Privacy Statement
A statement of privacy will be given (see intervention) after the health question.
|
The participant reads this statement after being asked one of eight health question for example.
"We will not share or sell this personal health information with anyone.
We will comply with all HIPPA regulations regarding the protection of your data."
|
Experimental: Benefit + Privacy statement
A statement of benefit and privacy will be given (see intervention) after the health question.
|
The statement reads "Accurately answering this will increase the likelihood of a correct diagnosis.
We will not share or sell this personal health information with anyone.
We will comply with all HIPPA regulations regarding the protection of your data."
|
Experimental: Risk + privacy statement
A statement of risk and privacy will be given (see intervention) after the health question.
|
The statement reads "Inaccurately answering this will increase the likelihood of an incorrect diagnosis.
We will not share or sell this personal health information with anyone.
We will comply with all HIPPA regulations regarding the protection of your data."
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Patient truthfulness - biometric mouse-movement distance
Time Frame: The time frame of data collection will be from when the survey is opened by the participant until it is completed and submitted. This will take 10 - 20 minutes.
|
The measure of the distance (mm) the mouse travels to the response.
|
The time frame of data collection will be from when the survey is opened by the participant until it is completed and submitted. This will take 10 - 20 minutes.
|
Patient truthfulness - biometric mouse-movement time
Time Frame: The time frame of data collection will be from when the survey is opened by the participant until it is completed and submitted. This will take 10 - 20 minutes.
|
The measure of the time (ms) the mouse travels to the response.
|
The time frame of data collection will be from when the survey is opened by the participant until it is completed and submitted. This will take 10 - 20 minutes.
|
Patient truthfulness Weight - answer adjustment from -5 to 5 for each health question
Time Frame: The time frame of data collection will be from when the survey is opened by the participant until it is completed and submitted. This will take 10 - 20 minutes.
|
Participants will be given a summary of their answers from their health questions in a read-only format and asked to indicate how over- or understated each initial response was (e.g., "You indicated that your current weight is 185 lbs.
How overstated or understated is that value?") on a scale from -5 (understated) to 5 (overstated).
The absolute value of their response represents the extent to which participants' initial response deviated from the truth.
Participant's actual response to the health questions are NOT an outcome measure but rather how much they adjust their answer on a scale of (-5 to +5).
|
The time frame of data collection will be from when the survey is opened by the participant until it is completed and submitted. This will take 10 - 20 minutes.
|
Patient truthfulness Height - answer adjustment from -5 to 5 for each health question
Time Frame: The time frame of data collection will be from when the survey is opened by the participant until it is completed and submitted. This will take 10 - 20 minutes.
|
Participant will be shown a summary of their answer from their health question (What is your height in inches) and then respond to how much they under represented the information (-5) to being accurate (0) to overstated the information (+5).
Participant response will be on a sliding scale -5 to +5
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The time frame of data collection will be from when the survey is opened by the participant until it is completed and submitted. This will take 10 - 20 minutes.
|
Patient truthfulness Drink Alcohol - answer adjustment from -5 to 5 for each health question
Time Frame: The time frame of data collection will be from when the survey is opened by the participant until it is completed and submitted. This will take 10 - 20 minutes.
|
Participant will be shown a summary of their answer from their health question (How many days out of the last 2 weeks did you drink alcohol?
(1 = 0 time; 6 = 13-14 times)) and then respond to how much they under represented the information (-5) to being accurate (0) to overstated the information (+5).
Participant response will be on a sliding scale -5 to +5
|
The time frame of data collection will be from when the survey is opened by the participant until it is completed and submitted. This will take 10 - 20 minutes.
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Patient truthfulness Drug Activity - answer adjustment from -5 to 5 for each health question
Time Frame: The time frame of data collection will be from when the survey is opened by the participant until it is completed and submitted. This will take 10 - 20 minutes.
|
Participant will be shown a summary of their answer from their health question (How often a month do you use other substance such as marijuana, cocaine, ecstasy, or other drugs (1 = never; 6 = all the time)) and then respond to how much they under represented the information (-5) to being accurate (0) to overstated the information (+5).
Participant response will be on a sliding scale -5 to +5
|
The time frame of data collection will be from when the survey is opened by the participant until it is completed and submitted. This will take 10 - 20 minutes.
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Patient truthfulness Prescription Use - answer adjustment from -5 to 5 for each health question
Time Frame: The time frame of data collection will be from when the survey is opened by the participant until it is completed and submitted. This will take 10 - 20 minutes.
|
Participant will be shown a summary of their answer from their health question (How often a month do you use Rx or non-Rx medications to excessive amounts?
(1 = never; 6 = all the time)) and then respond to how much they under represented the information (-5) to being accurate (0) to overstated the information (+5).
Participant response will be on a sliding scale -5 to +5
|
The time frame of data collection will be from when the survey is opened by the participant until it is completed and submitted. This will take 10 - 20 minutes.
|
Patient truthfulness Cigarette Smoking- answer adjustment from -5 to 5 for each health question
Time Frame: The time frame of data collection will be from when the survey is opened by the participant until it is completed and submitted. This will take 10 - 20 minutes.
|
Participant will be shown a summary of their answer from their health question (When was the last time you smoked a cigarette?
(1 = 6+ weeks ago to 6 = today)) and then respond to how much they under represented the information (-5) to being accurate (0) to overstated the information (+5).
Participant response will be on a sliding scale -5 to +5
|
The time frame of data collection will be from when the survey is opened by the participant until it is completed and submitted. This will take 10 - 20 minutes.
|
Patient truthfulness Exercise Activity- answer adjustment from -5 to 5 for each health question
Time Frame: The time frame of data collection will be from when the survey is opened by the participant until it is completed and submitted. This will take 10 - 20 minutes.
|
Participant will be shown a summary of their answer from their health question (How many days in the last 2 weeks did you engage in more than 30 min exercise?
(1 = 13-14 times; 6 = 0 times)) and then respond to how much they under represented the information (-5) to being accurate (0) to overstated the information (+5).
Participant response will be on a sliding scale -5 to +5
|
The time frame of data collection will be from when the survey is opened by the participant until it is completed and submitted. This will take 10 - 20 minutes.
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Patient truthfulness Sexual Activity - answer adjustment from -5 to 5 for each health question
Time Frame: The time frame of data collection will be from when the survey is opened by the participant until it is completed and submitted. This will take 10 - 20 minutes.
|
Participant will be shown a summary of their answer from their health question (How many times did you engage in sexual activity in the last month with another individual?
(1 = 0; 6 = 20+ times)) and then respond to how much they under represented the information (-5) to being accurate (0) to overstated the information (+5).
Participant response will be on a sliding scale -5 to +5
|
The time frame of data collection will be from when the survey is opened by the participant until it is completed and submitted. This will take 10 - 20 minutes.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Gender
Time Frame: The time frame of data collection will be from when the survey is opened by the participant until it is completed and submitted. This will take 10 - 20 minutes.
|
Participants will record their gender they identify with - Male or Female
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The time frame of data collection will be from when the survey is opened by the participant until it is completed and submitted. This will take 10 - 20 minutes.
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Mark Keith, PhD, Brigham Young University
Publications and helpful links
General Publications
- Buhrmester M, Kwang T, Gosling SD. Amazon's Mechanical Turk: A New Source of Inexpensive, Yet High-Quality, Data? Perspect Psychol Sci. 2011 Jan;6(1):3-5. doi: 10.1177/1745691610393980. Epub 2011 Feb 3.
- Levy AG, Scherer AM, Zikmund-Fisher BJ, Larkin K, Barnes GD, Fagerlin A. Prevalence of and Factors Associated With Patient Nondisclosure of Medically Relevant Information to Clinicians. JAMA Netw Open. 2018 Nov 2;1(7):e185293. doi: 10.1001/jamanetworkopen.2018.5293.
- Jerrold L. Litigation, legislation, and ethics. When patients lie to their doctors. Am J Orthod Dentofacial Orthop. 2011 Mar;139(3):417-8. doi: 10.1016/j.ajodo.2010.09.004. No abstract available.
- Petty RE, Cacioppo JT. The elaboration likelihood model of persuasion. Advances in Experimental Social Psychology. 1986;19:123-205
- Lowry PB, Moody G, Vance A, Jensen M, Jenkins J, Wells T. Using an elaboration likelihood approach to better understand the persuasiveness of website privacy assurance cues for online consumers. Journal of the American Society for Information Science and Technology. 2012;63(4):755-776
- Kahneman D, Tversky A. Prospect theory: an analysis of decision under risk. Econometrica. 1979;47(2):263-291
- Jenkins JL, Proudfoot J, Valacich J, Grimes GM, Nunamaker Jr JF. Sleight of hand: identifying concealed information by monitoring mouse-cursor movements. Journal of the Association for Information Systems. 2019;20(1):1-32
- Keith MJ, Thompson SC, Hale J, Lowry PB, Greer C. Information disclosure on mobile devices: re-examining privacy calculus with actual user behavior. International Journal of Human-Computer Studies. 2013;71(12):1163-1173
- DePaulo BM, Kashy DA, Kirkendol SE, Wyer MM, Epstein JA. Lying in everyday life. J Pers Soc Psychol. 1996 May;70(5):979-95.
- Argo JJ, White K, Dahl DW. Social comparison theory and deception in the interpersonal exchange of consumption information. Journal of Consumer Research. 2006;33(1):99-108
- Marchewka A, Jednorog K, Falkiewicz M, Szeszkowski W, Grabowska A, Szatkowska I. Sex, lies and fMRI--gender differences in neural basis of deception. PLoS One. 2012;7(8):e43076. doi: 10.1371/journal.pone.0043076. Epub 2012 Aug 29.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 19-059
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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