Trial · NCT07882459
Registered outcomes16
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
1 to 16 of 16
Download this page as JSON| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Participant Completion of the iMGi Workflow | From baseline (T0) to final follow-up (T5), approximately 10 months | Proportion of enrolled participants who complete the full structured preventive care workflow, including the scheduled visits from baseline (T0) through the final follow-up (T5). Calculated as the number of participants completing the workflow divided by the total number of enrolled participants, expressed as a percentage. |
| Primary | Adherence to Predefined iMGi Workflow Steps | Across study visits from T0 through T5, approximately 10 months | Proportion of study visits during which all predefined steps of the structured iMGi preventive care workflow are performed as planned. Calculated as the number of visits with complete adherence to the predefined workflow steps divided by the total number of evaluable visits, expressed as a percentage. |
| Secondary | Change in Bleeding on Interdental Brushing (BOB) Index | Baseline (T0) and final follow-up (T5), approximately 10 months | Change in interdental gingival bleeding between baseline (T0) and final follow-up (T5), assessed using the Bleeding on Interdental Brushing (BOB) Index. Results are expressed as the percentage of evaluated interdental sites presenting bleeding following interdental brushing. |
| Secondary | Longitudinal Changes in BOB Score | Baseline (T0) through final follow-up (T5), approximately 10 months | BOB Scores, expressed as percentages, measured across study visits to describe the trajectory of interdental gingival bleeding during implementation of the structured preventive care workflow. |
| Secondary | Change in Full Mouth Bleeding Score (FMBS) | Baseline (T0) and final follow-up (T5), approximately 10 months | Change in the percentage of periodontal sites presenting bleeding on probing, assessed using the Full Mouth Bleeding Score (FMBS). |
| Secondary | Change in Full Mouth Plaque Score (FMPS) | Baseline (T0) and final follow-up (T5), approximately 10 months | Change in the percentage of tooth surfaces presenting plaque, assessed using the Full Mouth Plaque Score (FMPS). |
| Secondary | Change in Periodontal Pocket Depth (PPD) | Baseline (T0) and final follow-up (T5), approximately 10 months | Change in periodontal probing depth, measured in millimetres using periodontal charting. |
| Secondary | Change in Gingival Margin Level | Baseline (T0) and final follow-up (T5), approximately 10 months | Change in gingival margin position, measured in millimetres relative to the cementoenamel junction. |
| Secondary | Change in Oral Health Motivation Scale (OHMS) Scores | Baseline (T0) and final follow-up (T5), approximately 10 months | Change in questionnaire scores assessing oral health motivation and related behaviours. |
| Secondary | Change in Health Belief Model (HBM) Questionnaire Scores | Baseline (T0) and final follow-up (T5), approximately 10 months | Change in questionnaire scores assessing health beliefs and perceptions related to oral health and preventive behaviours. |
| Secondary | Self-Reported Adherence to Interdental Cleaning | During the study, from T0 through T5, approximately 10 months | Participant-reported adherence to recommended interdental cleaning practices during follow-up. |
| Secondary | Change in Perceived Oral Health and Well-Being (POHW) Scores | Baseline (T0) and final follow-up (T5), approximately 10 months | Change in patient-reported perceived oral health and well-being questionnaire scores. |
| Secondary | Patient Satisfaction With the Preventive Care Workflow | During the study, up to T5, approximately 10 months | Patient satisfaction questionnaire scores describing participants' experiences with the structured preventive care workflow. |
| Secondary | Researcher Evaluation of Workflow Implementation | During the study, through T5, approximately 10 months | Researcher evaluation scores describing the implementation and practical application of the structured preventive care workflow. |
| Secondary | Workflow Usability Indicators | During the study, through T5, approximately 10 months | Descriptive indicators of the perceived usability and practical integration of the structured workflow in routine clinical care. |
| Secondary | Adherence to Protocol Steps | Across study visits from T0 through T5, approximately 10 months. | Descriptive measures of adherence to predefined study procedures and workflow steps across participating centres. |
Source ClinicalTrials.govtrials-2026-11-12-0.5.0
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
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