Skip to main content
Clinical Trials/NCT05316766
NCT05316766
Completed
Not Applicable

Multi-user Touch Surfaces for Promoting Social Participation and Self-efficacy in Upper-limb Stroke Rehabilitation

Universidade da Madeira1 site in 1 country12 target enrollmentMarch 29, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Social Interaction
Sponsor
Universidade da Madeira
Enrollment
12
Locations
1
Primary Endpoint
Action Research Arm Test (change between three time frames )
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

The purpose of this study is to compare the efficacy of conventional therapy with a framework intervention for upper limb motor rehabilitation based on the promotion of self-efficacy and social participation/interaction through a multi-user touch surface

Detailed Description

After signing the written informed consent about participating in the study, participants will be assessed for exclusion criteria and their motor, social and depression skills prior to intervention. After this, they will undergo a 12 sessions treatment for 4 weeks in groups of three, randomly distributed for a control group and experimental group. At the end of the intervention, participants will be assessed in the same manner as before the intervention. One month after the end of the intervention, participants will be assessed for follow-up.

Registry
clinicaltrials.gov
Start Date
March 29, 2022
End Date
August 31, 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Sergi Bermúdez i Badia

Professor

Universidade da Madeira

Eligibility Criteria

Inclusion Criteria

  • Stroke survivor

Exclusion Criteria

  • Unable to write and read
  • Hemispatial neglect
  • Previous upper limb motor deficits/lesions that still interfere with function
  • History of drugs/alcohol abuse
  • Aphasia with difficulties understanding oral communication and/or unability to express orally
  • Token equal or under 17
  • ARAT score lower than 10 or higher than 54
  • Botulinic toxin treatment in the last 4 months
  • Beck's Depression Inventory higher than 31

Outcomes

Primary Outcomes

Action Research Arm Test (change between three time frames )

Time Frame: Assessment (before intervention), Reassessment (after 12 x 45 minutes sessions, 3 sessions per week) and Follow-up (1 month after the end of intervention)

Hand Function

Dynamometer (change between three time frames)

Time Frame: Assessment (before intervention), Reassessment (after 12 x 45 minutes sessions, 3 sessions per week) and Follow-up (1 month after the end of intervention)

Strength

Motor Activity Log (change between three time frames)

Time Frame: Assessment (before intervention), Reassessment (after 12 x 45 minutes sessions, 3 sessions per week) and Follow-up (1 month after the end of intervention)

Quantity and Quality of movement everyday activities

Reaching Performance Scale in Stroke (change between three time frames)

Time Frame: Assessment (before intervention), Reassessment (after 12 x 45 minutes sessions, 3 sessions per week) and Follow-up (1 month after the end of intervention)

Quality of movement

Stroke Self-Efficacy Questionnaire (change between three time frames)

Time Frame: Assessment (before intervention), Reassessment (after 12 x 45 minutes sessions, 3 sessions per week) and Follow-up (1 month after the end of intervention)

Self-efficacy, minimum 0 maximum 130, higher score means better outcome

Box and Blocks (change between three time frames)

Time Frame: Assessment (before intervention), Reassessment (after 12 x 45 minutes sessions, 3 sessions per week) and Follow-up (1 month after the end of intervention)

Coordination

Nine Hole Peg Test (change between three time frames)

Time Frame: Assessment (before intervention), Reassessment (after 12 x 45 minutes sessions, 3 sessions per week) and Follow-up (1 month after the end of intervention)

Fine motor skills

Fugl-Meyer Assessment (change between three time frames)

Time Frame: Assessment (before intervention), Reassessment (after 12 x 45 minutes sessions, 3 sessions per week) and Follow-up (1 month after the end of intervention)

Range of movement

Secondary Outcomes

  • Beck's Depression (change between three time frames)(Assessment (before intervention), Reassessment (after 12 x 45 minutes sessions, 3 sessions per week) and Follow-up (1 month after the end of intervention))
  • Social Interaction category of ''Functional Limitation Profile'' (specific name of the scale) (change between three time frames)(Assessment (before intervention), Reassessment (after 12 x 45 minutes sessions, 3 sessions per week) and Follow-up (1 month after the end of intervention))

Study Sites (1)

Loading locations...

Similar Trials