Digital Reinforcement of Motivational Interviewing Micro-Skills Among Primary Care Healthcare Professionals
NCT07922837, Not applicable, Active not recruiting, National University Polyclinics, Singapore
Trial 10
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
| Field | Value | Source |
|---|---|---|
| Title | Digital Reinforcement of Motivational Interviewing Micro-Skills Among Primary Care Healthcare Professionals | ClinicalTrials.gov |
| NCT number | NCT07922837 | ClinicalTrials.gov |
| Status | Active not recruiting | ClinicalTrials.gov |
| Phases | Not applicable | ClinicalTrials.gov |
| Enrollment | 57 participants, actual | ClinicalTrials.gov |
| Lead sponsor | National University Polyclinics, Singapore | ClinicalTrials.gov |
| Conditions | Hypertension (Without Type 2 Diabetes Mellitus) | ClinicalTrials.gov |
| Interventions | Digital Nudges for Motivational Interviewing (MI) Micro-Skills Reinforcement | ClinicalTrials.gov |
| First posted | 2026-11-06 | ClinicalTrials.gov |
| Last updated | 2026-11-06 | ClinicalTrials.gov |
Registered outcomes 5
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description | Source |
|---|---|---|---|---|
| Primary | Change From Baseline in Systolic Blood Pressure | Baseline and up to 12 weeks after the index consultation | Change in systolic blood pressure (mmHg) from the index consultation (baseline) to the most recent routine-care blood pressure reading taken at least four weeks after the index consultation and within twelve weeks of the index consultation among eligible hypertensive patients managed by participating healthcare professionals. | ClinicalTrials.gov |
| Secondary | Acceptability of Intervention Measure (AIM) | Baseline and Week 17 (end of intervention) | Perceived acceptability of the structured reinforcement programme on Motivational Interviewing (MI) micro-skills, measured using the four-item Acceptability of Intervention Measure (AIM). Anticipated acceptability will be assessed at baseline prior to intervention commencement, and experienced acceptability will be assessed after completion of the 17-week intervention. Higher scores indicate greater perceived acceptability. | ClinicalTrials.gov |
| Secondary | Intervention Appropriateness Measure (IAM) | Baseline and Week 17 (end of intervention) | Perceived appropriateness of the structured reinforcement programme on Motivational Interviewing (MI) micro-skills, measured using the four-item Intervention Appropriateness Measure (IAM). Anticipated appropriateness will be assessed at baseline prior to intervention commencement, and experienced appropriateness will be assessed after completion of the 17-week intervention. Higher scores indicate greater perceived appropriateness. | ClinicalTrials.gov |
| Secondary | Feasibility of Intervention Measure (FIM) | Baseline and Week 17 (end of intervention) | Perceived feasibility of the structured reinforcement programme on Motivational Interviewing (MI) micro-skills, measured using the four-item Feasibility of Intervention Measure (FIM). Anticipated feasibility will be assessed at baseline prior to intervention commencement, and experienced feasibility will be assessed after completion of the 17-week intervention. Higher scores indicate greater perceived feasibility. | ClinicalTrials.gov |
| Secondary | Confidence in Applying Motivational Interviewing (MI) | Baseline and Week 17 (end of intervention) | Self-reported confidence in applying Motivational Interviewing (MI) in routine clinical practice, measured using a study questionnaire administered before and after the intervention. | ClinicalTrials.gov |
Outcomes 0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as | Source |
|---|
Results by group 0
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units | Source |
|---|
Participant flow 0
How many started, completed or left each group, period by period.
| Period | Milestone | Group | Participants | Units counted | Source |
|---|
Adverse events 0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
| Type | Event | Organ system | Group | Affected | At risk | Events | Source |
|---|
Adverse event totals 0
The totals the trial posted for each group.
| Total | Group | Affected | At risk | Source |
|---|
Papers 0
The papers the trial lists on ClinicalTrials.gov.
| PMID | Listed as | Source |
|---|
Grants 0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
| Project | Title | Principal investigators | Organization | Funder | Fiscal years | Source |
|---|
Trial comparisons 0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
| Comparison | Source |
|---|
Tests 0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
| Test | Named as | Source |
|---|
Source 5
| Field | Value | Source |
|---|---|---|
| Release | trials-2026-11-12-0.4.0 | ClinicalTrials.gov |
| Release manifest SHA-256 | 0f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4 | ClinicalTrials.gov |
| Registry capture | 2026-11-12 | ClinicalTrials.gov |
| Results copy, AACT | 2026-03-23 | ClinicalTrials.gov |
| NIH clinical studies file | 2026-11-13 | ClinicalTrials.gov |
Release trials-2026-11-12-0.4.0
ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.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.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
ClinicalTrials.gov: none stated ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
NIH RePORTER's clinical studies and project files: Public domain (NIH RePORTER)