Skip to main content
Clinical Trials/NCT02955303
NCT02955303
Completed
Not Applicable

The Feasibility of TECH: Tablet Enhancement of Cognition and Health, Cognitive Training Using Touchscreen Tablet Gaming Applications, for Healthy Older Adults - a Pilot Randomized Control Trial

Assuta Hospital Systems1 site in 1 country10 target enrollmentNovember 2016
ConditionsHealthy Adults

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Healthy Adults
Sponsor
Assuta Hospital Systems
Enrollment
10
Locations
1
Primary Endpoint
Feasibility information
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

This study assess the feasibility of novel cognitive intervention utilizing tablet apps (TECH protocol: Tablet Enhancement of Cognition and Health) in terms of relevance, adherence, suitable challenges, training time etc. for healthy older adults. Older adults with normal cognition will be randomly allocated to the TECH protocol (experimental group) or the control group (no treatment). Assessments will be administered pre and post the 6-week TECH protocol by assessors blind to group allocation.

Detailed Description

A pre-post pilot study will be conducted. Participants will be referred to the study from 'Maccabi Healthcare Services' by family physicians and geriatric physician of 'Maccabi Healthcare Services Central District'. The majority of TECH protocol training will take place in the participants' home as self-practice. The assessment and weekly group meetings will take place at clinics of Maccabi Healthcare Services in the Central District. A Helsinki approval (#2016009) has already been obtained. Participants will receive information regarding the study and if eligible will sign a consent form, undergo the screening and then the pre-intervention assessments. Then they will receive the TECH protocol, and following the intervention a second assessment will be performed.

Registry
clinicaltrials.gov
Start Date
November 2016
End Date
August 2019
Last Updated
6 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Assuta Hospital Systems
Responsible Party
Principal Investigator
Principal Investigator

Zvi Buckman

Dr. Zvi Buckman

Assuta Hospital Systems

Eligibility Criteria

Inclusion Criteria

  • Aged 65 and above.
  • Without cognitive decline (score 26 points or above in MoCA).
  • ) live independently in the community (as reported by the participants, regarding their independence in BADL and IADL, excluding motor difficulties which are not caused due to neurological conditions or lack of performance with no changes compared to the past.
  • Have normal or corrected vision and hearing.
  • Speak, write and read Hebrew.
  • Able to understand and follow use of the touchscreen of a tablet after initial demonstration.

Exclusion Criteria

  • Experience severe depressive symptoms (10 points or more in The Geriatric Depression Scale).
  • Are diagnosed with dementia, or other neurological or psychiatric condition (such as stroke, Parkinson's disease).

Outcomes

Primary Outcomes

Feasibility information

Time Frame: 7 minutes

Information regarding: Adherence - the percentage of session attendance out of the six weekly group sessions; Compliance - assessed by the total self-training hours a week, which was taken from participant's daily logs and iPad Screen time information. Satisfaction from the intervention was rated by the participants after completion of the TECH intervention.

Secondary Outcomes

  • The Tower of Hanoi (ToH) task(10 minutes)
  • The Montreal Cognitive Assessment(10 minutes)
  • WebNeuro(20 minutes)

Study Sites (1)

Loading locations...

Similar Trials