Skip to main content
OpenTrials
Completed

NCT Number: NCT01365858

Virtual Action Planning in Stroke: a Control Rehabilitation Study

* Background : The general experience with the Virtual Reality application approach suggests that this treatment concept is promising in stroke rehabilitation * Purpose : In shopping activity in a real supermarket and in simulated with the investigators virtual shopping simulation (VAP-S = virtual action planning supermarket), the investigators will compare people who had undergone a stroke who receive conventional rehabilitation or virtual training in VAP-S.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

CHU Bordeaux, Bordeaux, France

Loading trial locations.

About this study

The objective of this study is firstly to examine the effectiveness of using virtual reality-based training VAP-S on the ability to run errands in a real supermarket in individuals with stroke. Virtual environment provide useful way to explore planning and secondly to examine the effectiveness of using VR in the assessment of cognitive planning for patients. A virtual supermarket was designed in which participants carried out a task close to daily activities: a test of shopping list. Of the 70 subjects (7 centres), 35 randomly allocated to the control group, and the other 35 subjects randomly allocated to the experimental group. Subjects will be evaluated by a therapist who will not be involved in the training program and did not know about the subject's group assignment.

Statistical analysis : We will calculate descriptive statistics for the clinical characteristics of each group. We will use to compare the baseline demographic characteristics, the pretraining and posttraining variables between groups, independent-samples t-tests for means and Chi-square tests for frequencies. A significance level of 0.05 is set for all analyses.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Adults
  • 1 to 18 months after stroke
  • Without dementia or previous clinical stroke
  • With executive impairment (Grefex battery)
  • Barthel score equal or more than 40
  • With cognitive disability leading to specific rehabilitation
  • Given and informed consent

Exclusion criteria

  • dementia or severe psychiatric disease
  • epilepsy
  • disorder of consciousness
  • visual agnosia
  • severe visual impairment

Treatment and study plan

rehabilitation

Other

The experimental group patients receive rehabilitation by training "Virtual Action Planning - Supermarket" on a computer 45 minutes 5 times a week during a 2-week period. The control group will receive similar duration cognitive rehabilitation (no extra computer training) during this period (problem solving and occupational therapy).

Primary outcomes

  1. Ability to perform shopping test in real supermarket (all items collected and all actions needed done)

    Time frame: After rehabilitation (day 16)

Secondary outcomes

  1. Time to perform all actions in real shop; performance in virtual shopping simulation (number of items, time, inappropriate actions); user and caregiver satisfaction.

    Time frame: Before (day 1) and after (day16) rehabilitation

Sponsors and collaborators

Lead sponsor

University Hospital, Bordeaux

Other

Registry information

Official study title

Effectiveness of Virtual Reality-based Cognitive Training in Daily Living in Stroke Patients Using Virtual Action Planning Supermarket (VAP-S)

Acronym: VAPS REHAB

Important dates

Study start
2011
Primary completion
2014
Study completion
2014
First posted
Jun 3, 2011
Registry last updated
May 14, 2026

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.

Published trials that share one or more normalized conditions with this study.