The Feasibility of a Virtual/Home-based OA Treatment Program in Older Adults With OA and Multimorbidity
NCT07921563, Not applicable, Not yet recruiting, Dartmouth-Hitchcock Medical Center
Trial 10
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
| Field | Value | Source |
|---|---|---|
| Title | The Feasibility of a Virtual/Home-based OA Treatment Program in Older Adults With OA and Multimorbidity | ClinicalTrials.gov |
| NCT number | NCT07921563 | ClinicalTrials.gov |
| Status | Not yet recruiting | ClinicalTrials.gov |
| Phases | Not applicable | ClinicalTrials.gov |
| Enrollment | 50 participants, estimated | ClinicalTrials.gov |
| Lead sponsor | Dartmouth-Hitchcock Medical Center | ClinicalTrials.gov |
| Conditions | Osteoarthritis of the Knee | ClinicalTrials.gov |
| Interventions | Home-based exercise and weight management program | ClinicalTrials.gov |
| First posted | 2026-11-06 | ClinicalTrials.gov |
| Last updated | 2026-11-06 | ClinicalTrials.gov |
Registered outcomes 6
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description | Source |
|---|---|---|---|---|
| Primary | Knee Injury and Osteoarthritis Outcomes Score (KOOS) | 3 and 6 months | A valid, reliable, and responsive scale developed for use in studies of knee problems including osteoarthritis. | ClinicalTrials.gov |
| Primary | Prospective preference assessment | Baseline | Descriptive feasibility outcome, a 5 point likert scale used to determine patient willingness to participate in the research. | ClinicalTrials.gov |
| Secondary | Use, dose, and frequency of analgesics | 3 and 6 months | Patient-reported counts of the use, dose, and frequency of pain medications used, including non-steroidal anti-inflammatory drugs | ClinicalTrials.gov |
| Secondary | Self-reported current weight | 3 and 6 months | Patients will be asked to self report their current weight at the defined time points | ClinicalTrials.gov |
| Secondary | Participant satisfaction and adherence | 3 and 6 months | Patient satisfaction will be measured using a 5 point Likert scale for a series of questions aimed at perceived effectiveness of the intervention, ease of use and likeliness of continuing in the intervention | ClinicalTrials.gov |
| Secondary | The Physical Activity Scale for the Elderly (PASE) | 3 and 6 months | A recommended and reliable assessment for physical activity in older adults that has demonstrated positive correlation with Actigraph monitor data | 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 1
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 |
|---|---|---|---|---|---|---|
| P20GM161873 | Center for Aging with Serious Illness (CASI) | Volandes, Angelo; Goldstein, Nathan E | DARTMOUTH-HITCHCOCK CLINIC | NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES | 2026 | NIH RePORTER |
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)