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Clinical Trials/NCT03383549
NCT03383549
Completed
Not Applicable

Home-rehabilitation Protocol in Elderly Subjects With Mild Cognitive Impairment (MCI) Based on Information and Communications Technology (ICT) and Serious Games for Cognitive and Physical Training. Games for Older Adults Active Life (GOAL)

Fondazione Don Carlo Gnocchi Onlus1 site in 1 country60 target enrollmentJanuary 1, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cognitive Dysfunction
Sponsor
Fondazione Don Carlo Gnocchi Onlus
Enrollment
60
Locations
1
Primary Endpoint
Comparison between the cognitive ability measured at the end of the treatment (time point 2 months) and at the screening time point
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

Aging is often associated with pathological pathway such as in Mild Cognitive Impairment (MCI), and that pathway may be associated to a high risk of dementia.

Tools for early identification of functional and cognitive decline and effectiveness of treatments in counteracting the loss of functionality to preserve MCI subjects autonomy, have been widely debated in recent years.

In literature, the importance of combined cognitive and physical training is also recognized (Karssemeijer E, 2017).

Moving from the above mentioned findings and considerations, the aim of GOAL project is to test a newly developed tele-rehabilitation platform to monitor and preserve functional and cognitive abilities in individuals affected by Mild Cognitive Impairment (MCI).

Participants will be enrolled and randomly assigned to the tele-rehabilitation (GOAL group) or usual care program (control group). A dedicated application will be developed for the GOAL group. Thanks to the application, the participant will access different contents, such as serious games to train cognitive abilities (Anguera et al,2013) and physical training video lessons to endorse daily activity. Each participant of GOAL group will be provided with a tablet, with the application installed on it, and an internet connection (if needed).

Detailed Description

30 patients will be allocated in the treatment arm (Telerehabilitation program, GOAL group) by randomization. Randomization will be applied with a ratio of 1:1. The Telerehabilitation program is conceived as a combined protocol to train both cognitive and physical domains. Participants will be requested to perform the cognitive training three times weekly and physical training two times weekly, on alternate days. The subject will access the Telerehabilitation contents by using a web application configured on a touchscreen notebook, that will be provided to each participant by the research institute. Physical exercises are going to be chosen according to adaptive physical activity model, and each session will be made up of eleven exercises, divided in three categories: warm-up, strengthening and stretching/relaxation. The participants will perform the exercises according to instructions received in a sequence of videos. Every session will last 30 minutes. Cognitive training will be based on BrainHQ exercises (BrainHQ, Posit Science,USA) which are characterized by adaptive control of the difficulty levels. The chosen exercises aim to train different cognitive domains including: attention, executive function, memory, processing speed, reasoning, and visuospatial memory. Each session will last 20 minutes, and will include four different types of exercise. While enrolled in the 8 weeks program, participants will also be requested to wear an actigraph. The actigraph will be placed on the non-dominant arm and will be used to monitor daily activity and sleep quality. At the end of the tele-rehabilitation program, participants will undergo a final assessment.

Registry
clinicaltrials.gov
Start Date
January 1, 2018
End Date
June 30, 2019
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Unreliable communication (eg, foreign language or aphasia)
  • Severe visual or auditory deficit, not reversible, to the extent that it compromises the interaction with the operator and the usage of ICT instrumentation.
  • Presence of neurological and/or psychiatric disorders (Hamilton scale \>12) that might interfere with cognitive status
  • Left-handed individuals
  • Level of education \<3 years
  • History of substance abuse (nicotine excluded)
  • Having relapsing systemic disease and presence of major head trauma
  • Frank dementia
  • MMSE \<24

Outcomes

Primary Outcomes

Comparison between the cognitive ability measured at the end of the treatment (time point 2 months) and at the screening time point

Time Frame: At the screening time point and after 2 months of treatment

Changes in cognitive ability will be assessed by Montreal Cognitive Assessment (MoCA) Test (Conti et al., 2014)

Secondary Outcomes

  • Copy and Recall of Rey's Figure(At the screening time point and after 2 months of treatment)
  • Verbal fluency task(At the screening time point and after 2 months of treatment)
  • Serious Game test(At the screening time point and after 2 months of treatment)
  • Maintenance or improvement of the physical activity(At the screening time point and after 2 months of treatment)
  • Stroop Test(At the screening time point and after 2 months of treatment)

Study Sites (1)

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