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NCT06606600
Impacts of Kebbi Robot Intervention for Older Adults With Mild Dementia
NA trial testing Intensive Kebbi robot interventions in Mild Cognitive Impairment (MCI) in 136 participants. Currently enrolling.
30 July 2025
Quick facts
| Lead sponsor | National Tainan Junior College of Nursing |
|---|---|
| Phase | NA |
| Status | Recruiting now |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | triple |
| Primary purpose | supportive care |
| Enrollment | 136 |
| Start date | 3 February 2025 |
| Primary completion | 30 July 2025 |
| Estimated completion | 30 July 2025 |
| Sites | 2 locations across Taiwan |
Drugs / interventions tested
- Intensive Kebbi robot interventions
Conditions studied
- Mild Cognitive Impairment (MCI) — all drugs for Mild Cognitive Impairment (MCI) →
Sponsor
National Tainan Junior College of Nursing
Who can join
65 and older, any sex, with Mild Cognitive Impairment (MCI). Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The goal of this clinical trial is to examine the immediate and sustained effects of an intensive Kebbi robot intervention on cognitive functions, heart rate variability (HRV), and psychological changes for older adults with mild dementia in long-term care (LTC). The main questions it aims to answer are: * Are intensive Kebbi robot interventions effective in improving cognitive functions, HRV, and psychological changes for older adults with mild dementia in LTC? * What are the participants\' experiences and perceptions after intensive Kebbi robot interventions? Researchers will compare intensive Kebbi robot interventions to a control group (receiving usual activity) to see if they are effective in improving cognitive functions, HRV, and psychological changes in older adults with mild dementia in LTC. Participants will: * Participants in the intensive Kebbi robot interventions will receive 30 minutes, thrice weekly, for 12 weeks. Participants in the control group will receive the usual activity. * The outcome measures will be conducted at three time points: before the intervention (T0), immediately after the end of the intervention (T1), and one month after the end of the intervention (T2). * Outcome measurements include the cognitive outcomes: Mini-Mental State Examination (MMSE), Montreal Cognitive Assessment (MoCA), Finger Tapping Test (FTT); heart rate variability (HRV); psychological changes: the Geriatric depression scale-short form (GDS-SF), the UCLA Loneliness Scale Version 3 (UCLA- Version 3), and the Friendship scale.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT06606600
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Other National Tainan Junior College of Nursing trials
Trials by the same sponsor.
- NCT05957861 — Exploring the Effectiveness to Web-based Exercise Among Community-dwelling Adults With High Body Fat · NA · completed
- NCT05949710 — Explore the Relationship Between Heart Rate Variability, Body Mass Index, Inflammation, and Insulin Resistance. · NA · completed
- NCT05580263 — Different Order of Concurrent Training on Improving Visceral Adipose Tissue and Insulin Resistance. · NA · completed
- NCT05102201 — Effect of the Group-based Paro Intervention on Physiological and Psychological Outcomes · NA · completed
- NCT05215275 — Comparison of Different Exercise Trainings on Heart Rate Variability · NA · completed
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT06606600 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by National Tainan Junior College of Nursing
- Last refreshed: 28 May 2025
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06606600.
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