Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
28 participants
INTERVENTIONAL
2019-09-03
2019-11-29
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Public Health Impact of Unilateral Spatial Neglect
NCT05792969
Effects of Community Occupational Therapy in Older Patients With Dementia and Their Caregivers.
NCT00295152
Effects of Multidomain Intervention on Cognitive Function in Community-dwelling Elderly
NCT06180161
Reappraising Intergeneration Relationships in Dementia Caregiving
NCT03584568
Exploring the Impact of Dementia Prevention Programs Using Robots as Intervention Tools on Community Elderly
NCT06984458
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
NON_RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Experimental group
Experimental group receive a 10-wk diversified community-based reablement service.
community-based reablement service
Experimental group receive a 10-wk diversified community-based reablement service including group exercise, cognitive training, health education for 1.5 hours, and individualized reablement for 1.0 hour.
Control group
Control group receive a 10-wk multicomponent training.
multicomponent training
control group receive a 10-wk multicomponent training including 1.5-hr group intervention (group exercise, cognitive training, and health education) and 1.0-hr placebo intervention.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
community-based reablement service
Experimental group receive a 10-wk diversified community-based reablement service including group exercise, cognitive training, health education for 1.5 hours, and individualized reablement for 1.0 hour.
multicomponent training
control group receive a 10-wk multicomponent training including 1.5-hr group intervention (group exercise, cognitive training, and health education) and 1.0-hr placebo intervention.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* speaking with Chinese or Taiwanese
* DEMMI score of 39-67
Exclusion Criteria
* unable to understand or follow one step instruction
65 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
CY Song
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
CY Song
assistant professor
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
ChenYi Song
Role: PRINCIPAL_INVESTIGATOR
National Taipei University of Nursing and Health Sciences
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
National Taipei University of Nursing and Health Sciences
Taipei, , Taiwan
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
19-060-B
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.