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Completed

NCT Number: NCT04803799

Effects of an Exergame Focused on Cognitive-motor Interference on the Cognitive and Motor Capacities of Older Adults

Ageing is accompanied by a high risk of developing physical or cognitive impairments, as well as a decrease in abilities to perform two tasks simultaneously, contributing to loss of autonomy.

Interventions based on the performance of cognitive-motor dual tasks show positive effects on cognitive, physical and emotional development on dual-tasking capabilities. Exergames, interactive serious games combining physical activity and technology, are a certain type of cognitive-motor dual task training. These exergames appear to be cognitively effective, discussed on a physical level, not studied on dual task functions. It is likely that a dual task cognitive-motor with the support of a exercise leads to the same benefits as training without the need for special support.

In addition, the exergames benefit from specific features such as a good immersion and a playful aspect that increase the participant's adhesion. Moreover, the level of security of this type of programme has been little studied. It is likely that cognitive-motor dual tasks training supported by an exercise programme leads to few undesirable events and good adherence.

Many of the recommendations specific needs gaming state that it is important to develop systems that respond to the needs specific to the population concerned in order to be effective. Within the laboratory HAVAE has been developed a tool, the "virtual carpet":

association between a video-projected scene and a monitoring system of position of the participants. This system makes it possible to use as a grid of play the cartography and iconography of the City of Limoges. The investigators suppose that this emphasis on local heritage will encourage the participants leaving their homes, thereby increasing their level of physical activity and their quality of life.

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Key information

Conditions

Age range

75 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Résidence Autonomie CASSEAUX, Limoges, France

Loading trial locations.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

A person over 75 years of age who :

  • resides in one of the two Municipal Autonomy Residences (RAM) of the City of Limoges (Durkheim or Casseaux), or a member of a senior club of the communal social action centre
  • has normal or corrected vision and hearing

Exclusion criteria

Person presenting :

  • psychiatric disorders or neurological pathologies (cardiovascular accidents, Parkinson's disease, Alzheimer's, dementia) diagnosed
  • taking medication that affects walking or balance
  • a need for technical assistance (double cane-crutch, walker)
  • an inability to carry out the proposed training programme
  • person unable to understand the Protocol

Treatment and study plan

Training Programme

Other

Cognitive-motor dual task exercises corresponding to associations between different motor tasks and different cognitive tasks.

Primary outcomes

  1. Postural control under dual-task condition change

    Time frame: Week 3, Week 17

    assessed by posturography (mm/s)

Secondary outcomes

  1. Mental inhibition under dual-task condition change

    Time frame: Week 3, Week 17, Week 31

    assessed by Stroop test time (s)

  2. Mental inhibition under dual-task condition change

    Time frame: Week 3, Week 17, Week 31

    assessed by Stroop test errors (n)

  3. Mental inhibition change single-task condition

    Time frame: Week 3, Week 17, Week 31

    assessed by Stroop test time (s)

  4. Mental inhibition change single-task condition

    Time frame: Week 3, Week 17, Week 31

    assessed by Stroop test errors (n)

  5. Mental flexibility change

    Time frame: Week 3, Week 17, Week 31

    assessed by TMT time (s)

  6. Mental flexibility change

    Time frame: Week 3, Week 17, Week 31

    assessed by Stroop test errors (n)

  7. Working memory change

    Time frame: Week 3, Week 17, Week 31

    assessed by 2N-Back test errors (n)

  8. Mobility change

    Time frame: Week 3, Week 17, Week 31

    assessed by TUG time (s)

  9. Balance change

    Time frame: Week 3, Week 17, Week 31

    assessed by BBS score

  10. Fear of falling

    Time frame: Week 3, Week 17, Week 31

    assessed by FES-I score

  11. Postural control under single-task condition change

    Time frame: Week 3, Week 17, Week 31

    assessed by posturography (mm/s)

  12. Reported physical activity level change

    Time frame: Week 3, Week 17, Week 31

    assessed by QAPPA score

  13. Traqued physical activity level change

    Time frame: Week 3, Week 17, Week 31

    assessed by embeded Armband

  14. City exploration change

    Time frame: Week 17, Week 31

    assessed by the city's points of interest visits

  15. Quality of life change

    Time frame: Week 3, Week 17, Week 31

    assessed by EQ5D5L score

  16. Safety features of the training programme

    Time frame: Week 17

    number, nature, severity and causes of the occurrence of adverse events during the intervention

  17. Compliance

    Time frame: Week 17

    assessed by number of sessions carried out

  18. Drop-out

    Time frame: Week 17

    assessed by the number of participants who do not complete the program

  19. Motivation change

    Time frame: Week 3, Week 17, Week 31

    assessed by EMAPS score

Sponsors and collaborators

Lead sponsor

University Hospital, Limoges

Other

Registry information

Acronym: INCOME

Important dates

Study start
2021
Primary completion
2022
Study completion
2022
First posted
Mar 18, 2021
Registry last updated
Aug 1, 2025

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.

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