Remote Testing in Abbiategrasso (RTA) (RTA)

March 15, 2022 updated by: Antonio Guaita, MD, Fondazione Golgi Cenci

Feasibility Study on Remote Cognitive Assessment With Older People. A Counter-balanced Crossover Trial.

The remote cognitive assessment has the advantage of reaching people despite the restrictions due to the pandemic, so it is of fundamental importance both in the treatment of dementia and the research context. The scientific literature on the feasibility, acceptability and validity of remote neuropsychological assessment provides promising indications. However, the limitations related to access and familiarity with technologies in elderly populations, and to methodological aspects (e.g. the not-controlled environment, the validity of the remote assessment compared to the in-person assessment) remain to be clarified. For the present observational feasibility study, 58 older adults (65-85 years), randomly extracted among 93 eligible participants, will be recruited among donors of our Brain Bank. Participants will undergo both face-to-face and remote testing (via phone calls or videoconferencing) sessions in a counterbalanced cross-over design. The study will target (1) the recruitment rate in a study on remote testing, (2) the acceptability of remote cognitive tests and the procedures for delivering remote testing, (3) the comparability between remote and face-to-face performances on neuropsychological tests.

Study Overview

Status

Completed

Detailed Description

In February and March 2021, the 237 donors of our Brain Bank, aged between 65 and 98 and living at home, were interviewed by telephone. The purpose of the survey was to collect information on how they were experiencing the isolation linked to the pandemic in the last year, on health conditions and sleep, daily habits (nutrition, movement, leisure), use of the Internet and social networks as a way to maintain contact with one's family-friend network and experiences of loneliness (Rolandi et al, 2020). In this context, the willingness to participate in a study on remote cognitive assessment by phone, personal computer or tablet was explored.

The sample size was calculated to estimate differences between testing conditions, i.e. face-to-face and remote testing (telephone or videoconference). A sample size of 52 is required to detect an effect size of 0.40 at 0.80% of power, in a paired-sample test with a normal distribution. We planned an increase in sample size of 6 participants, because the expected drop-out rate is 10% due to possible acute clinical conditions interfering with the participation in the study, or death.

For the present observational feasibility study, 58 older adults (65-85 years), randomly extracted among 93 eligible participants, will be recruited among donors of the Brain Bank who previously have expressed the willingness to adhere to the study. Participants will undergo both face-to-face and remote testing sessions in a counterbalanced cross-over design. Each individual will undergo a comprehensive neuropsychological assessment consisting of a set of cognitive tests (memory, attention, etc) administered remotely via telephone calls or videoconferencing and face-to-face. Participants will be randomly allocated to one of the two conditions (remote first or face-to-face first). Each participant will take part to the second evaluation (remote or face-to-face) 8 weeks later. To reduce learning effect bias and intra-rate variability, this procedure will be counterbalanced so that half of the participants first experience the face-to-face interaction and the other half will initially receive the videoconference administration.

Study Type

Observational

Enrollment (Actual)

58

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Milan
      • Abbiategrasso, Milan, Italy, 20081
        • Golgi Cenci Foundation

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

65 years to 85 years (Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

In February and March 2021, the 237 donors of the Abbiategrasso Brain Bank, aged between 65 and 98 and living at home, were interviewed by telephone. The purpose of the survey was to collect information on how they were experiencing the isolation linked to the pandemic in the last year (Rolandi et al, 2020). In this context, the willingness to participate in a study on remote cognitive assessment by phone, personal computer or tablet was explored. For the present observational feasibility study, 58 older adults (65-85 years), randomly extracted among 93 eligible participants, will be recruited among donors of the Abbiategrasso Brain Bank who previously have expressed the willingness to adhere to the study.

Description

Inclusion Criteria:

  • willingness to adhere to the study
  • age between 65 and 85
  • normal cognition

Exclusion Criteria:

  • dementia, psychiatric or neurological diagnosis
  • presence of a memory disorder with impact on the daily life reported by the person or detected by the interviewer
  • previously scheduled follow-up of the Brain Bank

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: Case-Crossover
  • Time Perspectives: Prospective

Cohorts and Interventions

Group / Cohort
Group 1
Remote evaluation first: participants will undergo a comprehensive neuropsychological assessment administered remotely via telephone calls or videoconferencing. Each participant will take part to the second evaluation (face-to-face) 8 weeks later.
Group 2
Face-to-face evaluation first: participants will undergo a comprehensive neuropsychological assessment administered face-to-face. Each participant will take part to the second evaluation (remotely via telephone calls or videoconferencing) 8 weeks later.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Recruitment rate
Time Frame: Day 0
The primary outcome is the recruitment of the 58 Brain Bank donors in our study on remote cognitive assessment. Fifteen days after the informed consent is sent, the healthcare assistant will conduct telephone calls to receive confirmation of participation in a remote cognitive assessment study from the donors who previously had expressed their willingness to adhere. The healthcare assistant will collect information about the reason of refusal if any (i.e. not interested, health problems, away from home for holidays). It will also asked confirmation of the modality preferred for the remote assessment, i.e. by phone, tablet or computer.
Day 0

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Acceptability of remote cognitive tests among aged individuals (+65 years).
Time Frame: Day 1 and Month 2
Immediately following each session of cognitive evaluation (both remotely and face-to-face) participants completed an acceptability questionnaire previously developed to evaluate the response to computerised cognitive tasks in both the clinic-based and home-based setting. Participants will be required to rate the enjoyability, level of anxiety, engagement, duration and repeatability of the tasks, rating them on a five-point Likert scale: 1, not at all; 2, a little bit; 3, neutral; 4, slightly; 5, very much. The questionnaire comprises the following questions: Did the test make you anxious? Did you enjoy the test? Did you find the test interesting? Would you be happy to repeat the test? What did you think about the duration of the test?
Day 1 and Month 2

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Comparison between remote and face-to-face performances on the Montreal Cognitive Assessment (MoCA) Audiovisual
Time Frame: Day 1 and Month 2
The MoCA Audiovisual is the version of the MoCA test used for video administration with little adaptation. It is a screening test including 5-word learning (attention), animal semantic fluency (language, executive function), 6-item orientation, and delayed recall (memory). The visual section (trail making, clock drawing and the cube copy) is displayed on the video using the share screen option (range 0-30).
Day 1 and Month 2
Comparison between remote and face-to-face performances on the MoCA 5-minute
Time Frame: Day 1 and Month 2
The MoCA 5-minute is a brief version of the MoCA test with the visual elements removed and suitable for telephone administration. It is a screening test including 5-word learning (attention), animal semantic fluency (language, executive function), 6-item orientation, and delayed recall (memory). The MoCA 5-minute has been translated in Italian and it is commonly used in clinical setting (range 0-15).
Day 1 and Month 2
Comparison between remote and face-to-face performances on the Rey Auditory Verbal Learning Test (RAVLT)
Time Frame: Day 1 and Month 2
The RAVLT evaluates verbal learning and memory in young and older adults. It is designed as a list-learning paradigm in which the subject hears a list of 15 nouns and is asked to recall as many words from the list as possible. After a 15 minutes delay (performing interference non-verbal tasks), the participant is immediately asked to recall the words from the list. The RAVLT provides immediate (sum of words recalled on the 5 learning trials; range 0-75) and delayed recall scores (sum of the words recalled after 15 min; range 0-15), with higher scores indicating better performance on verbal learning and long-term memory.
Day 1 and Month 2
Comparison between remote and face-to-face performances on the Digit span forward and backward
Time Frame: Day 1 and Month 2
Digit span forward and backward are two subtests of the Wechsler Adult Intelligence Scale, assessing short-term memory and working memory respectively. Participants are asked to repeat sequences of numbers of increasing length in straight order (Digit span forward) or reverse order (Digit span backward). Performances are reported as span scores (the maximum number of digits correctly produced forwards or backwards by the subjects) (range 0-9), with higher scores indicative of better performance on short-term memory and working memory.
Day 1 and Month 2
Comparison between remote and face-to-face performances on the alternate phonemic/semantic fluency test
Time Frame: Day 1 and Month 2
The alternate phonemic/semantic fluency test measures spontaneous verbal production, executive function, processing speed and memory. It consists of three subtests: letter-cued (phonemic) fluency, category-cued (semantic) fluency and alternate phonemic/semantic fluency. The subtests are administered in the following order: phonemic, semantic and alternate fluency. In the first, the subject is asked to produce words beginning with a specified letter (F, A and S). In the second, one is asked to produced words belonging to a specified category (colours, animals and fruits). The score is obtained by the sum of the correct responses (range 0-…) within 60 seconds, with higher scores indicating better performances. In the third, the subjects have to alternate letter-cued words with category-cued words as follows: trial (1) letter A and Colours; trial (2) letter F and Animals; trial (3) letter S and Fruits. Three trials are given, each lasting 60 seconds.
Day 1 and Month 2
Comparison between remote and face-to-face performances on the Verbal reasoning test
Time Frame: Day 1 and Month 2
Verbal reasoning test evaluates the individual's ability to reason, i.e. solve problems, draw inferences and classify, based on previous knowledge.The test consists of four subtests: differences (for instance: what is the difference between glass and plate?), proverbs (for instance: what is the meaning of "The dress does not make the priest"?), nonsense (what's wrong or what's wrong with the following story?) and classifications (for instance: please, state the likeness between Milan, Rome, Naples and Venice). The score of items is attributed on the basis of predefined criteria, so that subtest scores varies between 0 and 15 (total range score 0-60), with higher scores indicative of better performance on verbal reasoning.
Day 1 and Month 2
Comparison between remote and face-to-face performances on the Constructional praxis
Time Frame: Day 1 and Month 2
Copy figure tasks are generally included in most of the common screening tests and battery administered remotely, although the high level of variability between studies. The Constructional praxis test cannot be administered by telephone, but can be drawn during the videoconference and displayed in front of the camera. Subjects are requested to copy images representing bi-dimensional and three-dimensional shape (range 0-16), with higher scores indicative of better performance on constructional ability.
Day 1 and Month 2
Comparison between remote and face-to-face performances on the Reading the Mind in the Eyes Test (RME)
Time Frame: Day 1 and Month 2
The term Theory of Mind (ToM) refers to the abilities to attribute mental states to others and to predict, describe, and explain behaviour on the basis of such mental state. ToM abilities are involved in social functioning and are affected in neurodegenerative diseases. The RME evaluates the cognitive component of ToM in adult and older people. The test consists of 36 black and white photographs depicting the eye region of adults, young and old people of both sexes. The subject is asked to indicate the term among four adjectives placed under the photograph, best describing the emotion expressed in the image (range 0-36). To limit the effect of the linguistic competences, a glossary is available to the subjects including definitions and clarifications for each of the words associated with the photos. To adapt the administration to the remote modality, the images will be projected on the shared screen.
Day 1 and Month 2

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Roberta Vaccaro, MSc, Fondazione Golgi Cenci

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

June 21, 2021

Primary Completion (Actual)

November 30, 2021

Study Completion (Actual)

December 31, 2021

Study Registration Dates

First Submitted

November 2, 2021

First Submitted That Met QC Criteria

November 15, 2021

First Posted (Actual)

November 26, 2021

Study Record Updates

Last Update Posted (Actual)

March 16, 2022

Last Update Submitted That Met QC Criteria

March 15, 2022

Last Verified

March 1, 2022

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

IPD Plan Description

The data may be made available to third parties as aggregated data.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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