Dementia (Diagnosis)

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Review clinical trials related to Dementia (Diagnosis). Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
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Status: Not yet recruiting

Merton Music Therapy Community-based Dementia Project

The goal of this single arm interventional, pre-post study is to learn about the feasibility and impact of group music therapy sessions for people living with dementia in two different community settings. This research will answer the following questions: 1. What is the impact of the music therapy groups upon attendees (people with dementia and informal carers) and does this differ between the two settings? 2. What is the impact of the music therapy groups upon staff and culture in the settings (day centre and memory hub staff)? 3. Is it feasible to conduct the study in these two settings? (recruitment, retention, attendance, delivery, data collection) 4. What are the barriers and facilitators to implementation in each setting? Participants will attend at weekly a music therapy group for a period of 10 weeks, either at the Merton Memory Hub run by Alzheimer's Society or at Eastways Day Centre run by Merton Council (Adult Social Care). These sessions will be led by a fully qualified, HCPC registered music therapist with experience working with people living with dementia. The music programme will be designed to promote engagement, social connection, enjoyment and personal identity with the overall aim to support quality of life, emotional regulation and the relationship quality between the person living with dementia and their carer. Data collection will involve mixed methods, such as quantitative validated questionnaires about wellbeing, loneliness, relationship quality between the carer and patient. These will be asked to both the person living with dementia and the carer. The music therapist will also conduct an observational Music in Dementia Assessment Scale on the behaviour of the participants living with dementia during the music therapy sessions. Qualitative data will be a semi-structured interview of about 20-30 mins to discuss with the participants, staff included, about their experiences once the programme is finished.

Participants needed: 28
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Anglia Ruskin UniversityUpdated: Jul 29, 2026
Eligibility criteria

With a diagnosis of dementia (or the informal/family carer to someone with a dia... [+3]

Lacking capacity to provide informed consent and no consultee available [+4]

Status: Not yet recruiting

Speech-Based Artificial Intelligence for Detection of Dementia in Danish Patients (DetectAI)

The goal of this observational study is to learn if an artificial intelligence (AI)-based speech analysis tool can identify which patients with memory problems need specialist evaluation at a memory clinic. The main questions it aims to answer are: Can the AI model accurately distinguish between patients who need referral to a memory clinic (those with dementia or Mild Cognitive Impairment) and patients who don't (those with normal cognition or memory problems from other causes like depression)? Which speech patterns and cognitive test features are most useful for making this distinction? Researchers will compare speech recordings and cognitive test results from patients diagnosed with dementia or MCI to those from patients with normal cognition or non-neurodegenerative cognitive impairment to see if the AI model can reliably predict who needs specialist dementia care. Participants will: Complete standard cognitive tests at the memory clinic Perform structured speech tasks while being audio-recorded Receive their usual clinical evaluation and diagnosis from memory clinic specialists The results of this study will help develop a tool that can assist doctors in making faster, more accurate decisions about which patients need specialist dementia evaluation, potentially leading to earlier diagnosis and better patient outcomes.

Participants needed: 440
Trial details
Age: 50+Biological sex: AllType: ObservationalSponsor: Zealand University HospitalUpdated: May 5, 2026Locations: 1
Eligibility criteria

Age > 50 years [+9]

Significantly impaired vision or hearing (to the extent that the patient cannot... [+16]

Status: Not yet recruiting

Mild Cognitive Impairment Community Screening and Early Intervention Via Stem Cell Therapy and Wearable Brain Computer Interface Device.

This study aims to evaluate the efficacy of community-based early detection and targeted interventions, including stem cell therapy and wearable non-invasive brain-computer interface (BCI) devices, for Mild Cognitive Impairment (MCI) in adults aged 55 years and older residing in U.S. urban and suburban communities. Primary objectives include assessing improvements in MCI detection rates, cognitive outcomes, and progression delay compared to standard care.

Participants needed: 600
Trial details
Phase: Early Phase 1Age: 55+Biological sex: AllType: InterventionalSponsor: Noah Tech, Corp.Updated: Mar 10, 2026Locations: 1
Eligibility criteria

Not listed

Status: Not yet recruiting

Loneliness as Risk Factor for Dementia

This study aims to determine whether loneliness is associated with a higher incidence of dementia in older adults with a prior diagnosis of mild cognitive impairment after 12 months of follow-up.

Participants needed: 300
Trial details
Age: 70+Biological sex: AllType: ObservationalSponsor: Consorci Sanitari de l'Alt Penedès i GarrafUpdated: Nov 26, 2025Locations: 1
Eligibility criteria

Not listed

Status: Not yet recruiting

Enhancing Utility of Neuropsychological Evaluation for Earlier and Effective Diagnosis of Dementia in Parkinson's Disease

Dementia is observed in 80% of people living with advanced stage Parkinson's disease, however, there are inadequate opportunities for early and effective diagnosis of dementia in current clinical practice. This study aims to identify whether a new tool called PDCogniCare, can improve detection of dementia in people living with Parkinson's disease, and to explore what factors might influence its use in healthcare services.

Participants needed: 275
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: The University of QueenslandUpdated: Aug 11, 2025
Eligibility criteria

People living with idiopathic Parkinson's disease, one year or more post-diagnos...

People with severe Parkinson's disease who aren't able to communicate [+1]