Trial · NCT06603727
Computerized Cognitive Rehabilitation of Patients With Cognitive Deficits Due to the Human Immunodeficiency Virus
NCT06603727, Not applicable, Unknown, Centre Hospitalier Universitaire Vaudois
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Computerized Cognitive Rehabilitation of Patients With Cognitive Deficits Due to the Human Immunodeficiency Virus. Trials, record NCT06603727. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT06603727
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Computerized Cognitive Rehabilitation of Patients With Cognitive Deficits Due to the Human Immunodeficiency Virus
- NCT number
- NCT06603727
- Status
- Unknown
- Phases
- Not applicable
- Enrollment
- 24 participants, estimated
- Lead sponsor
- Centre Hospitalier Universitaire Vaudois
- Conditions
- Human Immunodeficiency Virus, Cognitive Dysfunction
- Interventions
- Computerized Gaming Rehabilitation Program 1, Computerized Gaming Rehabilitation Program 2
- First posted
- 2024-09-19
- Last updated
- 2024-09-19
Source ClinicalTrials.gov
Registered outcomes37
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Change in subjective everyday life cognition after a 6 weeks period of gamified cognitive and physical training (program 1 vs program 2) | 6 weeks | Subjective executive function is measured by the Working Memory Questionnaire (WMQ), a 30-item, self-administered scale (score range from 0 to 120), addressing working memory (10 items), attention (10 items) and general executive function (10 items). The higher the score, the more it reflects cognitive difficulties. |
| Primary | Change in speed of information processing after a 6 weeks period of gamified cognitive and physical training | 6 weeks | Measured by the Symbol Digit Modalities Test (SDMT), scored from 0 to 110. The lower the score, the more it reflects cognitive difficulties. |
| Primary | Change in cognitive flexibility after a 6 weeks period of cognitive and physical training (program 1 vs program 2) | 6 weeks | Measured by the time completion of the Color Trails Test (CTT) in CTT1 and CTT2 (i.e., Flexibility Index: (CTT2-CTT1)/CTT1). The higher the Flexibility Index, the more it reflects cognitive difficulties. |
| Primary | Change in visuospatial short-term memory after a 6 weeks period of cognitive and physical training (program 1 vs program 2) | 6 weeks | Measured by the Brief Visuospatial Memory Test-Revised (BVMT-R), scored from 0 to 36. The lower the score, the more it reflects cognitive difficulties. |
| Secondary | Change in sustained attention after a 6 weeks period of gamified cognitive and physical training (program 1 vs program 2) | 6 weeks | Measured with the Test of Variables of Attention (TOVA) using the reaction time (RT) and the false alarm rate (FA). The higher the RT and FA, the more they reflect cognitive difficulties. |
| Secondary | Change in cognitive interference after a 6 weeks period of gamified cognitive and physical training (program 1 vs program 2) | 6 weeks | Measured with the Denis-Kaplan Color-Word interference Stroop test using the time completion in each condition. The higher the time completion, the more it reflects cognitive difficulties. |
| Secondary | Change in design fluency after a 6 weeks period of gamified cognitive and physical training (program 1 vs program 2) | 6 weeks | The Five-Point Test will be used to assess design fluency using the total number of design produced. The lower the score, the more it reflects cognitive difficulties. |
| Secondary | Change in cognitive flexibility after a 6 weeks period of gamified cognitive and physical training (program 1 vs program 2) | 6 weeks | A subtest of a custom-made tablet-based cognitive evaluation tool will measure cognitive flexibility. |
| Secondary | Change in visuo-spatial and verbal working memory control after a 6 weeks period of gamified cognitive and physical training (program 1 vs program 2) | 6 weeks | Measured using the Digit and Visuo-Spatial Span Test |
| Secondary | Change in divided attention after a 6 weeks period of gamified cognitive and physical training (program 1 vs program 2) | 6 weeks | Measured using the Test of Attentional Performance subtest Divided Attention |
1 to 10 of 37Source ClinicalTrials.gov
See all 37 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.
Papers23
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 comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests3
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 |
|---|---|---|
| Symbol Coding | Primary outcome | ConductCognition |
| Design Fluency Test | Secondary outcome | ConductCognition |
| Stroop Color-Word Test | Secondary outcome | ConductCognition |
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/NCT06603727
GET https://conductscience.org/api/trials/v1/NCT06603727/registered?page=2