Trial · NCT07883343
Effects of Adding a Registered Dietitian to Rural Community Healthy Behavior Support Services for Management of Type 2 Diabetes
NCT07883343, Not applicable, Completed, Indiana University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Effects of Adding a Registered Dietitian to Rural Community Healthy Behavior Support Services for Management of Type 2 Diabetes. Trials, record NCT07883343. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07883343
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Effects of Adding a Registered Dietitian to Rural Community Healthy Behavior Support Services for Management of Type 2 Diabetes
- NCT number
- NCT07883343
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 14 participants, actual
- Lead sponsor
- Indiana University
- Conditions
- Type 2 Diabetes
- Interventions
- Medical Nutrition Therapy Intervention
- First posted
- 2026-10-20
- Last updated
- 2026-10-20
Source ClinicalTrials.gov
Registered outcomes15
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Feasibility outcome: Community health events | From enrollment to end of study data collection at 8 months. | The number of community health events that occurred. |
| Primary | Feasibility outcome: Health screenings at community health events | From enrollment to end of study data collection at 8 months. | The number of individual health screenings that were conducted at the community health events. |
| Primary | Feasibility outcome: Recruitment Rate | From enrollment to 6 months. | The percent of individuals identified with type 2 diabetes from the health screenings that were recruited to receive MNT. |
| Primary | Feasibility outcome: Retention rate | From enrollment to end of study data collection at 8 months. | The number of individuals who completed the MNT interventions and follow up health screen. |
| Primary | Feasibility outcome: Adherence rate | From enrollment to end of MNT provision at 3 months. | The participant rate of adherence to MNT. |
| Secondary | Behavior outcome: Dietary intake | From enrollment to end of MNT at 3 months. | Dietary intake was collected using a 24 hour recall. |
| Secondary | Behavior outcome: Physical Activity | From enrollment to end of MNT at 3 months. | Physical activity was collected using a 7-day record. |
| Secondary | Health outcome: Height | From enrollment to end of study data collection at 8 months. | Height was self reported in inches. |
| Secondary | Health outcome: Weight | From enrollment to end of study data collection at 8 months. | Body weight (lbs) was measured using digital scale. |
| Secondary | Health outcome: Blood glucose | From enrollment to end of study data collection at 8 months. | Non fasting blood glucose (mg/dL) was measured by point of care instrument. |
1 to 10 of 15Source ClinicalTrials.gov
See all 15 registered outcomesOutcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
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 totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
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 comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
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/NCT07883343
GET https://conductscience.org/api/trials/v1/NCT07883343/registered