Skip to main content
OpenTrials
Completed

NCT Number: NCT07521865

Remote Technologies in Early Stages of Alzheimer's Disease

The investigators are adapting a tablet-based cognitive training program for Alzheimer's disease (AD) by focusing on specific cognitive components. It is aimed to demonstrate the feasibility, acceptability and usability of remote cognitive training in older adults with Mild Cognitive Impairment (MCI) and AD dementia. The study involves 36 participants in three groups, with a two-week intervention and focus groups for refinement.

Completed

Looking for future studies?

Notify Me

Key information

Age range

70 year–95 year

Sex eligibility

All sexes

Study type

Observational

Primary location

University Hospital of Old Age Psychiatry and Psychotherapy Bern

Bern, Canton of Bern, 3000, Switzerland

About this study

The investigators aim to extend a tablet-computer-based cognitive training (CT), fully developed in house (KEK 2020-00630), and tailored specifically towards a "typical-AD" cognitive component. This cognitive component is defined through a principal-component analysis (PCA), on which the domains affected by AD (episodic memory, spatial processing, semantic memory) have high loadings. The investigators moreover train working memory training to facilitate transfer effects. By including carers (family members, friends, professional carers) in the focus groups and the integration of help buttons, the investigators expect high adherence. The CT will be based on our ongoing study assessing the CT in people at risk for AD and subjective cognitive decline.

The investigators plan a small feasibility study in three different groups with a total of 36 elderly participants including cognitively normal (N=12), MCI (N=12), and mild-moderate stage dementia due to AD (N=12).

The focus will be on qualitative content analyses based on the results from the focus groups. The results from the first focus group sessions serve the selection, adaptation, and improvement of the CT before it is implemented in the two-week intervention including daily 30-minutes training sessions. A second focus group after the intervention will serve to gain additional insights from users and carers to further improve the CT. To complement this information, the investigators will quantitatively compare specific game parameters related to feasibility (number of levels achieved, numbers of sessions finished, number of dropouts), usability (time until reaching level 1 - learn duration, numbers of help button presses), and acceptability (game evaluation) between the three treatment groups.

The investigators aim to demonstrate that remote CT is possible in older adults with Mild Cognitive Impairment (MCI) and diagnosed AD dementia at home and in the care home setting by extending an existing tablet-based CT app with additional (easier) training levels, additional and detailed introductory material to also allow cognitively more severely impaired participants to conduct the CT with as little external support as possible. This study is considered as Risk Category A. The study intervention consists of a tablet-based CT, which does not provide any known risks for the participants.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Participants and study partners fulfilling all the following inclusion criteria are eligible for the study:

  • Informed Consent as documented by signature

Study partners:

  • Native or fluent German speaker

Participants:

  • Are able to give their consent to participate in the study
  • Age between 70 and 95 years
  • Native or fluent German speaker
  • Normal or corrected to normal vision and hearing
  • Ability to visit the study location repeatedly
  • MoCA score > 11

Exclusion criteria

  • Substance abuse
  • Severe neurological or psychiatric conditions (of note: patients with mild depressive symptoms not fulfilling the criteria for major depressive disorder will be recruited into the sample to better represent clinical reality)

Treatment and study plan

App-based cognitive training

Device

The cognitive training is administered remotely for 2 weeks daily (10 sessions). The participants play all 12 games for 8 minutes in each session.

Primary outcomes

  1. Feasibility of tablet-based cognitive training

    Time frame: Assessed at the end of the 2-week intervention (Day 10)

    Compliance rate (i.e.number of sessions completed)

Secondary outcomes

  1. Feasibility of tablet-based cognitive training

    Time frame: Assessed at the end of the 2-week intervention (Day 10)

    Number of levels achieved

  2. Usability

    Time frame: Assessed at the end of the 2-week intervention (Day 10)

    Time until accomplishment of the first level (learning time)

  3. Acceptability

    Time frame: Assessed within two weeks after day 10 of the intervention

    Qualitative evaluation of the games in a semi-structured interview (Focus group discussion). For each game, the same questions will be addressed in an open discussion.

  4. 2. Feasibility of tablet-based cognitive training

    Time frame: Assessed at the end of the 2-week intervention (Day 10)

    Number of drop-outs

Other outcomes

  1. Support 1

    Time frame: Assessed at the end of the 2-week intervention (Day 10)

    The extent of support needed from study partners (diary notes)

  2. Support 2

    Time frame: Assessed at the end of the 2-week intervention (Day 10)

    The number of sessions for which support was required (diary notes)

  3. Wellbeing

    Time frame: Assessed every day during the intervention, a couple of seconds before playing the games (answering the in-game question on the tablet precedes playing the scheduled session).

    Influence on mood and wellbeing (questionnaire)

  4. Evaluation of Games by Study Partner

    Time frame: Assessed every day after (within couple of minutes) each game of the intervention was played.

    Qualitative evaluation of the games in a semi-structured interview (Focus group discussion). For each game, the same questions will be addressed in an open discussion.

Sponsors and collaborators

Lead sponsor

University of Bern

Other

Registry information

Official study title

Remote Technologies in Early Stages of Alzheimer's Disease: Feasibility, Usability, and Acceptance of an App-based Cognitive Training

Important dates

Study start
2023
Primary completion
2026
Study completion
2026
First posted
Apr 13, 2026
Registry last updated
Jun 26, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.