Virtual Reality Tennis Training and Executive Function in Older Adults
NCT07916220, Not applicable, Completed, Beijing Sport University
Trial 10
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
| Field | Value | Source |
|---|---|---|
| Title | Virtual Reality Tennis Training and Executive Function in Older Adults | ClinicalTrials.gov |
| NCT number | NCT07916220 | ClinicalTrials.gov |
| Status | Completed | ClinicalTrials.gov |
| Phases | Not applicable | ClinicalTrials.gov |
| Enrollment | 39 participants, actual | ClinicalTrials.gov |
| Lead sponsor | Beijing Sport University | ClinicalTrials.gov |
| Conditions | Executive Function (Cognition), Healthy Older Adults | ClinicalTrials.gov |
| Interventions | Immersive Virtual Reality-Based Tennis Training, Virtual Reality Documentary Viewing | ClinicalTrials.gov |
| First posted | 2026-11-04 | ClinicalTrials.gov |
| Last updated | 2026-11-04 | ClinicalTrials.gov |
Registered outcomes 5
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description | Source |
|---|---|---|---|---|
| Primary | Inhibitory Control Assessed by Flanker Task Reaction Time | Baseline, immediately after the 4-week intervention, and 1 week after the intervention. | Reaction time (ms) for correct responses on congruent and incongruent trials of the Flanker task. Shorter reaction times indicate faster responses. | ClinicalTrials.gov |
| Primary | Cognitive Flexibility Assessed by the Number of Correct Responses on the More-Odd Shifting Task | Baseline, immediately after the 4-week intervention, and 1 week after the intervention. | The number of correct responses on the More-Odd shifting task. Higher numbers of correct responses indicate better task performance. | ClinicalTrials.gov |
| Primary | Cognitive Flexibility Assessed by More-Odd Shifting Task Reaction Time | Baseline, immediately after the 4-week intervention, and 1 week after the intervention. | Reaction time (ms) on the More-Odd Shifting task. Shorter reaction times indicate faster responses. Accuracy and reaction time are considered separate outcome measures. | ClinicalTrials.gov |
| Primary | Visuospatial Working Memory Assessed by Corsi Block-Tapping Task Block Span | Baseline, immediately after the 4-week intervention, and 1 week after the intervention. | Block Span is defined as the length of the last sequence correctly reproduced by the participant. Higher scores indicate better visuospatial working memory. | ClinicalTrials.gov |
| Primary | Visuospatial Working Memory Assessed by Corsi Block-Tapping Task Total Score | Baseline, immediately after the 4-week intervention, and 1 week after the intervention. | The Total Score was calculated as the product of the Block Span (the length of the last correctly reproduced sequence) and the total number of correctly reproduced sequences (correct trials) before the test was discontinued. Higher scores indicate better visuospatial working memory. | 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 2
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 |
|---|---|---|
| Corsi Block-Tapping Test | Primary outcome | ConductCognition |
| Eriksen Flanker Task | Primary outcome | ConductCognition |
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)