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NCT06666075Completed

Digital Reminiscence Therapy for Alzheimer's in Institutionalized People

Psychological and Mental Health of Institutionalized People Over 60 Years of Age With Alzheimer's: Effects of a Digital and Interactive Reminiscence Program.

Source: ClinicalTrials.gov · Last updated 15 Aug 2025

Brief summary (registry, in English)

Digital reminiscence therapy (DRT) is an innovative intervention designed to enhance the psychological health of institutionalized seniors with Alzheimer's disease. This approach utilizes digital tools to facilitate the sharing of personal memories and experiences, fostering social interaction and emotional engagement. By combining technology with therapeutic reminiscence techniques, DRT aims to stimulate cognitive function and improve mood, potentially alleviating symptoms of anxiety and depression commonly observed in this population. Research indicates that reminiscence therapy can lead to improvements in quality of life and overall well-being for individuals with dementia. The interactive nature of digital platforms encourages participation and allows caregivers to customize content based on the individual's preferences and history. As such, DRT not only serves to strengthen the connections between seniors and their pasts but also enhances their current social interactions, promoting a sense of identity and belonging. Overall, DRT represents a promising avenue for addressing the psychological needs of older adults with Alzheimer's in institutional settings, highlighting the potential benefits of integrating technology into therapeutic practices.

Status (registry)
Completed
Study type
Interventional
Enrollment
72 (actual)
First submitted
28 Oct 2024
Start date
20 Jan 2025
Primary completion date
14 Apr 2025
Lead sponsor
University of Jaén
NCT number
NCT06666075

What you commit to

  • Study type: Interventional
  • Participants enrolled: 72
  • From 20 Jan 2025 to the primary completion date, 14 Apr 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study design.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Diagnosis of other neurological or psychiatric conditions (such as vascular dementia, Parkinson's, or psychotic disorders) that may significantly interfere with the program's results.

Other

  • Patients in advanced stages of Alzheimer's with severe limitations in remembering autobiographical events or interacting with digital devices.
  • Vision, hearing, or fine motor problems that prevent the use of electronic devices in an appropriate manner, without the possibility of adaptation or assistance.
  • Individuals or legal representatives who are unable or unwilling to give informed consent.
  • Behaviors that may put the participant, staff, or other residents at risk when carrying out program activities.

Who the study is looking for

  • People over 60 years of age.
  • Confirmed diagnosis of mild or moderate Alzheimer's, where the patient still retains a certain degree of autobiographical memory.
  • People institutionalized in a geriatric care center or similar.
  • Level of cognitive impairment that allows understanding and basic interaction with digital tools.
  • Approval and signature of informed consent by the participant or his/her legal representative, demonstrating agreement to participate in the study.
  • Availability or access to devices (tablets or computers) provided by the study program or the care center.

Age in the registry: 60 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Miguel Ángel Fernández Sevilla
Coordinator of this site? Confirm its status
JaénSpainUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.