KCT0007184
Not yet recruiting
未知
A multicenter clinical study to evaluate the efficacy and feasibility of a 24-week multidomain intervention via a none-face-to-face platform in mild cognitive impairment
ConditionsMental and behavioural disorders
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Mental and behavioural disorders
- Sponsor
- Inha University Hospital
- Enrollment
- 100
- Status
- Not yet recruiting
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\. Subjects who completed end\-of\-study evaluation and participated in the preceding randomized controlled trial (RCT) Multidomain Interventions Via Face\-to\-face and Video Communication Platforms in Mild Cognitive Impairment.
- •2\. Being able to use the tablet PC through education, or having a person who can help a participant use the tablet PC.
- •3\. Having a reliable informant who could provide investigators with the requested information
- •4\. Provide written informed consent
Exclusion Criteria
- •1\. Major psychiatric illness such as major depressive disorders
- •2\. Dementia
- •3\. Other neurodegenerative disease (e.g., Parkinson's disease)
- •4\. Malignancy within 5 years
- •5\. Cardiac stent or revascularization within 1 year
- •6\. Serious or unstable symptomatic cardiovascular disease
- •7\. Other serious or unstable medical disease such as acute or severe asthma, active gastric ulcer, severe liver disease, or severe renal disease
- •8\. Severe loss of vision, hearing, or communicative disability
- •9\. Any conditions preventing cooperation as judged by the study physician
- •10\. Significant laboratory abnormality that may result in cognitive impairment
Outcomes
Primary Outcomes
Not specified
Similar Trials
Completed
Not Applicable
Multicenter clinical study to assess the effectiveness and safety of Aquala liner in total hip arthroplasty (THA)Hip disorders including osteoarthritisJPRN-UMIN000008730Graduate School of Medicine, The University of Tokyo760
Completed
Not Applicable
Multicenter clinical study to assess the effectiveness and safety of Trident II in total hip arthroplasty (THA)Osteoarthritis, Femoral head necrosis, Rheumatoid arthritis, fractureJPRN-UMIN000043715Stryker Japan K.K.191
Not yet recruiting
Not Applicable
Comparative clinical study of eye drops in dry eye syndromeDiseases of the eye and adnexaKCT0004516Kangbuk Samsung Medical Center60
Active, not recruiting
Phase 1
Multicentre clinical trial to evaluate the efficacy and safety of dexketoprofen trometamol (50 mg t.i.d.) versus ketorolac (30 mg t.i.d.) and placebo by intravenous route, as part of balanced analgesic therapy with morphine, followed by an oral dosing, in the treatment of postoperative paielective orthopedic surgery (hip arthroplasty)MedDRA version: 7.0Level: PTClassification code 10020096EUCTR2004-001373-26-ESaboratorios Menarini, S.A
Recruiting
Phase 2
Multicenter clinical trial to evaluate the efficacy of rituximab combination chemotherapy for children or AYAswith localized mature B-cell lymphomaJPRN-jRCTs041210104Sekimizu Masahiro100