Online Group-based Dual-task Training to Improve Cognitive Function of Community-dwelling Older Adults
NCT05573646, Not applicable, Completed, The University of Hong Kong
Trial 10
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
| Field | Value | Source |
|---|---|---|
| Title | Online Group-based Dual-task Training to Improve Cognitive Function of Community-dwelling Older Adults | ClinicalTrials.gov |
| NCT number | NCT05573646 | ClinicalTrials.gov |
| Status | Completed | ClinicalTrials.gov |
| Phases | Not applicable | ClinicalTrials.gov |
| Enrollment | 76 participants, actual | ClinicalTrials.gov |
| Lead sponsor | The University of Hong Kong | ClinicalTrials.gov |
| Conditions | Aging Well | ClinicalTrials.gov |
| Interventions | Dual-task training, Attention Control | ClinicalTrials.gov |
| First posted | 2022-10-10 | ClinicalTrials.gov |
| Last updated | 2024-08-23 | ClinicalTrials.gov |
Registered outcomes 27
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description | Source |
|---|---|---|---|---|
| Primary | Change from baseline subjective memory complaints at 6 weeks | Six weeks after baseline | Measured by Memory Inventory in Chinese. The sum of score ranges from 0 to 108, higher score indicates more memory complaints. | ClinicalTrials.gov |
| Primary | Change from baseline subjective memory complaints at 12 weeks | 12 weeks after baseline | Measured by Memory Inventory in Chinese. The sum of score ranges from 0 to 108, higher score indicates more memory complaints. | ClinicalTrials.gov |
| Primary | Change from baseline subjective memory complaints at 18 weeks | 18 weeks after baseline | Measured by Memory Inventory in Chinese. The sum of score ranges from 0 to 108, higher score indicates more memory complaints. | ClinicalTrials.gov |
| Secondary | Change from baseline cognitive status at 6 weeks | Six weeks after baseline | Measured by the Montreal Cognitive Assessment 5-Minutes (Hong Kong Version) (HK-MoCA 5-Min) protocol. The total score ranges from 0 to 30; a higher score indicates better cognitive status. | ClinicalTrials.gov |
| Secondary | Change from baseline cognitive status at 12 weeks | 12 weeks after baseline | Measured by the Montreal Cognitive Assessment 5-Minutes (Hong Kong Version) (HK-MoCA 5-Min) protocol. The total score ranges from 0 to 30; a higher score indicates better cognitive status. | ClinicalTrials.gov |
| Secondary | Change from baseline cognitive status at 18 weeks | 18 weeks after baseline | Measured by the Montreal Cognitive Assessment 5-Minutes (Hong Kong Version) (HK-MoCA 5-Min) protocol. The total score ranges from 0 to 30; a higher score indicates better cognitive status. | ClinicalTrials.gov |
| Secondary | Change from baseline working memory at 6 weeks | Six weeks after baseline | Measured by Digit Span Test. The longer the series, the better the condition. | ClinicalTrials.gov |
| Secondary | Change from baseline working memory at 12 weeks | 12 weeks after baseline | Measured by Digit Span Test. The longer the series, the better the condition. | ClinicalTrials.gov |
| Secondary | Change from baseline working memory at 18 weeks | 18 weeks after baseline | Measured by Digit Span Test. The longer the series, the better the condition. | ClinicalTrials.gov |
| Secondary | Change from baseline executive function at 6 weeks | Six weeks after baseline | Measured by Chinese version of the Victoria Stroop Test, with more time and errors as worse condition. | ClinicalTrials.gov |
| Secondary | Change from baseline executive function at 12 weeks | 12 weeks after baseline | Measured by Chinese version of the Victoria Stroop Test, with more time and errors as worse condition. | ClinicalTrials.gov |
| Secondary | Change from baseline executive function at 18 weeks | 18 weeks after baseline | Measured by Chinese version of the Victoria Stroop Test, with more time and errors as worse condition. | ClinicalTrials.gov |
| Secondary | Change from baseline lower-limb muscle strength at 6 weeks | Six weeks after baseline | Measured by the 5-times chair stand task. The longer the time participants use to finish the task, the poorer the performance. | ClinicalTrials.gov |
| Secondary | Change from baseline lower-limb muscle strength at 12 weeks | 12 weeks after baseline | Measured by the 5-times chair stand task. The longer the time participants use to finish the task, the poorer the performance. | ClinicalTrials.gov |
| Secondary | Change from baseline lower-limb muscle strength at 18 weeks | 18 weeks after baseline | Measured by the 5-times chair stand task. The longer the time participants use to finish the task, the poorer the performance. | ClinicalTrials.gov |
| Secondary | Change from baseline happiness at 6 weeks | Six weeks after baseline | Measured by the Chinese version of the 4-item Subjective Happiness Scale. The score is the average of the four items, and ranges from 1 to 7; a higher score indicates a higher happiness level. | ClinicalTrials.gov |
| Secondary | Change from baseline happiness at 12 weeks | 12 weeks after baseline | Measured by the Chinese version of the 4-item Subjective Happiness Scale. The score is the average of the four items, and ranges from 1 to 7; a higher score indicates a higher happiness level. | ClinicalTrials.gov |
| Secondary | Change from baseline happiness at 18 weeks | 18 weeks after baseline | Measured by the Chinese version of the 4-item Subjective Happiness Scale. The score is the average of the four items, and ranges from 1 to 7; a higher score indicates a higher happiness level. | ClinicalTrials.gov |
| Secondary | Change from baseline depressive symptoms at 6 weeks | Six weeks after baseline | Measured by the Patient Health Questionnaire-9. The scale ranged from 0 to 27, higher score indicates higher level of depressive symptoms. | ClinicalTrials.gov |
| Secondary | Change from baseline depressive symptoms at 12 weeks | 12 weeks after baseline | Measured by the Patient Health Questionnaire-9. The scale ranged from 0 to 27, higher score indicates higher level of depressive symptoms. | 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 1
The papers the trial lists on ClinicalTrials.gov.
| PMID | Listed as | Source |
|---|---|---|
| 40378407 | DERIVED | PubMed |
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 |
|---|---|---|
| Digit Span Test | Secondary outcome | ConductCognition |
| Stroop Color-Word Test | Secondary 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)