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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04489563
Other study ID # i-ACT elderly
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 1, 2017
Est. completion date May 12, 2019

Study information

Verified date July 2020
Source PXL University College
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

A mix-method cross-sectional feasibility study performed in five aged care institutes in Flanders, Belgium. A convenience sample of 48 aged persons was recruited and 12 supervisors (i.e. occupational therapy students and therapists).

Aged persons received a 20-30 minutes test with a technology-based system, i.e. intelligent Activity-based Client-centred Training system (i-ACT). The i-ACT consists of the Microsoft Kinect and adapted software in which movements can be recorded and training parameters can be set by supervisors.

During and after the test, the thinking aloud method was used. After the test, the Intrinsic Motivation Inventory, the System Usability Scale, and the Credibility/Expectancy Questionnaire were administered in the aged persons.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date May 12, 2019
Est. primary completion date May 12, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 65 Years and older
Eligibility Inclusion Criteria:

- a client of the participating centres

- cognitively able to understand and respond to questions

- follow up instructions

- understand and speak the Dutch language

Exclusion Criteria:

- severe spasticity that unables participants to perform exercises

- severe visual impairment (e.g. blindness, cataract, etc.)

- severe communication disorder that unables participants to understand and follow up instructions (e.g. aphasia, agnosia, etc.)

- persons who use electric wheelchairs who are not able to make a transfer towards a chair.

Study Design


Related Conditions & MeSH terms

  • Feasibility of a Technology-based System in Aged Person

Intervention

Device:
i-ACT
Performing exercises with an adapted motion detection device (i.ACT) for 20-30 minutes.

Locations

Country Name City State
Belgium Plankeweeke Hasselt Limburg
Belgium Begralim Riemst Limburg
Belgium Begralim Tongeren Limburg
Belgium DVC H. Catharina Zonhoven Limburg
Belgium WZC H. Catharina Zonhoven Limburg

Sponsors (1)

Lead Sponsor Collaborator
PXL University College

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary Intrinsic motivation Using the Intrinsic Motivation Inventory to record motivational aspects 30 minutes
Primary Usability of i-ACT Using the System Usability Scale to explore the usability of i-ACT in aged persons. The System Usability Scale consists of a 10 item questionnaire with five response options for respondents; from Strongly agree to Strongly disagree. The items scores are converted into a score from 0 (negative) to 100 (positive). A score of 72.5 or higher is considered good and above 85.0 is excellent. 10 minutes
Primary Credibility/expectancy Using the Credibility/Expectancy Questionnaire to research the credibility and expectancy of aged persons when using the i-ACT for physical activity. It is one test that consists of 2 subscales, i.e. credibility and expectancy, and scores range from 1 (totally not) to 9 (totally yes) and percentages. The percentages are converted to scores on a scale of 1 to 9/ The maximum score on each subscale is 27. A score of 13.5 is considered neutral, everything above 13.5 is positive while everything under 13.5 is considered negative. 10 minutes