Univeristy of Jordan Hospital, Dental Department
Amman, Jordan
NCT Number: NCT07370545
This study is a clinical trial designed to understand how the way a dentist presents tooth color options affects a patient's final choice for their dental treatment. The insvestigators know that patients often prefer lighter, "bleached" shades, but the process of choosing can be influenced by the order in which the shades are shown.
The insvestigators will randomly dividing participants into three groups. One group will see natural shades first, followed by bleached shades. A second group will see bleached shades first, followed by natural shades. The third group will see all shades at once.
The main goal is to measure how often patients change their mind (switch their choice) and by how much (the "jump" in lightness) depending on the order of presentation. The insvestigators will also use a questionnaire to see if a patient's self-consciousness about their smile affects how light of a shade they choose. The results will help dentists improve communication and ensure patients are truly satisfied with their final aesthetic decision.
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Notify Me18 year–65 year
All sexes
Interventional
Not applicable
Amman, Jordan
This is a prospective, single-center, three-arm parallel-group Randomized Controlled Trial (RCT) designed to rigorously investigate the cognitive bias known as the "order effect" in patient-driven tooth shade selection. The study aims to quantify the influence of sequential versus simultaneous shade guide presentation on final aesthetic preference and to correlate this choice with the patient's underlying psychosocial perception of their dental aesthetics.
Methodology: Participants seeking aesthetic dental treatment will be randomized (1:1:1) into three intervention groups:
Outcome Measures: The primary outcomes are the switching frequency and the magnitude of change (Delta L*) between initial and final selections in the sequential groups (A and B), and the comparison of the final proportion of bleached shade selections across all three groups. Secondary outcomes include the correlation between the Psychosocial Impact of Dental Aesthetics Questionnaire (PIDAQ) total score and the final selected shade's L* value, and the quantification of the Patient-Clinician Discrepancy using CIE Delta E00 between the patient's choice and an independent clinician's recommendation.
Significance: This study will provide evidence-based guidelines for clinical practice, moving beyond anecdotal preference recording to a structured, bias-mitigating approach to shared aesthetic decision-making. The integration of the PIDAQ and objective colorimetric analysis (Lab*) and Delta E00 will provide a novel, high-impact explanation for the observed preference for lighter shades.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Participants are first presented with the natural range of the VITA 3D-Master shade guide (1M1-5M3) to select an initial preference. Following this, the bleached shade tabs (0M1-0M3) are introduced, and participants are invited to finalize their choice. This procedure measures the "pull" toward lighter shades when introduced as a secondary option.
Participants are first presented with the bleached range of the VITA 3D-Master shade guide (0M1-0M3) to select an initial preference. Following this, the full natural range (1M1-5M3) is introduced, and participants are invited to finalize their choice. This procedure measures the stability of the bleached shade preference when natural alternatives are subsequently provided.
Participants are presented with the complete VITA 3D-Master shade guide, including both natural (1M1-5M3) and bleached (0M1-0M3) tabs, in a single session. Participants select their preferred shade from the entire range simultaneously. This serves as the control method to establish baseline preference without sequential bias.
Time frame: At the time of shade selection (Day 1)
The lightness (L*) value of the final tooth shade selected by the patient using the VITA 3D-Master guide. The VITA 3D-Master tabs will be converted to CIE Lab* coordinates based on established conversion tables. This measure assesses the final aesthetic preference across the three randomized groups.
Time frame: At the time of shade selection (Day 1)
The percentage of participants in the sequential groups (Group A and Group B) who change their initial shade selection after the second range of shade tabs is introduced. This measures the stability of the initial choice and the susceptibility to presentation bias.
Time frame: At the time of shade selection (Day 1)
The numerical difference in lightness (L*) between the patient's initial shade selection and their final shade selection in the sequential groups (Group A and Group B). A positive value indicates a "jump" toward a lighter shade, while a negative value indicates a shift toward a darker shade.
Time frame: Baseline (Day 1)
The correlation coefficient between the total score of the Psychosocial Impact of Dental Aesthetics Questionnaire (PIDAQ) and the final selected shade's L* value. Higher PIDAQ scores indicate a greater negative psychosocial impact of dental aesthetics.
Time frame: At the time of shade selection (Day 1)
The color difference (calculated using the CIE Delta E00 formula) between the patient's final selected shade tab and the independent clinician's professional recommendation. This quantifies the gap between patient desire and professional aesthetic judgment.
Time frame: At the time of shade selection (Day 1)
The color difference (calculated using the CIE Delta E 00 formula) between the patient's final selected shade tab and the objective natural tooth color measured by a spectrophotometer.
University of Jordan
Other
The Influence of Shade Guide Presentation Sequence and Psychosocial Factors on Patient Tooth Shade Selection: A Three-Arm Randomized Controlled Trial
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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