Trial · NCT03985852
Broadening the Reach, Impact, and Delivery of Genetic Services
NCT03985852, Not applicable, Completed, University of Utah; results first posted 2025-01-08
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Broadening the Reach, Impact, and Delivery of Genetic Services. Trials, record NCT03985852. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT03985852
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Broadening the Reach, Impact, and Delivery of Genetic Services
- NCT number
- NCT03985852
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 3,073 participants, actual
- Lead sponsor
- University of Utah
- Conditions
- Cancer, Risk Reduction Behavior
- Interventions
- Patient Directed Standard of Care
- First posted
- 2019-06-14
- Last updated
- 2025-09-22
- Results first posted
- 2025-01-08
Source ClinicalTrials.gov
Registered outcomes3
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Completion of Genetic Testing From Electronic Health Record | 1 month following pre-test genetic counseling | Percentage of patients who decide to receive genetic testing |
| Secondary | Completion of Pre-test Genetic Counseling From Electronic Health Record | 1 month after study invitation | Percentage of patients who decide to receive pre-test genetic counseling |
| Secondary | Adherence to Colonoscopy: Questionnaire | 8 weeks and 13 months from pre-test counseling | Adherence to colonoscopy: questionnaire data |
Source ClinicalTrials.gov
Outcomes3
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as |
|---|---|---|---|---|---|
| PRIMARY | Completion of Genetic Testing From Electronic Health Record | 1 month following pre-test genetic counseling | Participants | COUNT_OF_PARTICIPANTS | |
| SECONDARY | Completion of Pre-test Genetic Counseling From Electronic Health Record | 1 month after study invitation | Participants | COUNT_OF_PARTICIPANTS | |
| SECONDARY | Adherence to Colonoscopy: Questionnaire | 8 weeks and 13 months from pre-test counseling | Population is participants who completed pre-test genetic services and follow-up questionnaires. | Participants | COUNT_OF_PARTICIPANTS |
Source ClinicalTrials.gov
Results by group6
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units |
|---|---|---|---|---|---|
| Completion of Genetic Testing From Electronic Health Record | Patient Directed Standard of Care | 191 | Participants | ||
| Completion of Genetic Testing From Electronic Health Record | Enhanced Standard of Care | 206 | Participants | ||
| Completion of Pre-test Genetic Counseling From Electronic Health Record | Patient Directed Standard of Care | 400 | Participants | ||
| Completion of Pre-test Genetic Counseling From Electronic Health Record | Enhanced Standard of Care | 361 | Participants | ||
| Adherence to Colonoscopy: Questionnaire | Patient Directed Standard of Care | 17 | Participants | ||
| Adherence to Colonoscopy: Questionnaire | Enhanced Standard of Care | 24 | Participants |
Source ClinicalTrials.gov
Participant flow6
How many started, completed or left each group, period by period.
| Period | Milestone | Group | Participants | Units counted |
|---|---|---|---|---|
| Overall Study | STARTED | Patient Directed Standard of Care | 1,554 | |
| Overall Study | STARTED | Enhanced Standard of Care | 1,519 | |
| Overall Study | COMPLETED | Patient Directed Standard of Care | 400 | |
| Overall Study | COMPLETED | Enhanced Standard of Care | 361 | |
| Overall Study | NOT COMPLETED | Patient Directed Standard of Care | 1,154 | |
| Overall Study | NOT COMPLETED | Enhanced Standard of Care | 1,158 |
Source ClinicalTrials.gov
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals6
The totals the trial posted for each group.
| Total | Group | Affected | At risk |
|---|---|---|---|
| Total, all-cause mortality | Patient Directed Standard of Care | 0 | 1,554 |
| Total, all-cause mortality | Enhanced Standard of Care | 0 | 1,519 |
| Total, other adverse events | Patient Directed Standard of Care | 0 | 1,554 |
| Total, other adverse events | Enhanced Standard of Care | 0 | 1,519 |
| Total, serious adverse events | Patient Directed Standard of Care | 0 | 1,554 |
| Total, serious adverse events | Enhanced Standard of Care | 0 | 1,519 |
Source ClinicalTrials.gov
Papers3
The papers the trial lists on ClinicalTrials.gov.
Grants0
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.
None in this release.
Trial comparisons5
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
| Comparison | Source |
|---|---|
| Patient Directed Standard of Care vs Enhanced Standard of Care: Completion of Pre-test Genetic Counseling From Electronic Health Record | Trial comparisons |
| Patient Directed Standard of Care vs Enhanced Standard of Care: Completion of Genetic Testing From Electronic Health Record | Trial comparisons |
| Patient Directed Standard of Care vs Enhanced Standard of Care: Adherence to Colonoscopy: Questionnaire | Trial comparisons |
| Patient Directed Standard of Care vs Enhanced Standard of Care: deaths from any cause | Trial comparisons |
| Patient Directed Standard of Care vs Enhanced Standard of Care: serious adverse events | Trial comparisons |
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
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.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT03985852
GET https://conductscience.org/api/trials/v1/NCT03985852/registered