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Effects of Power Wheelchair Soccer for Individuals Presenting With Physical Impairments

Not Applicable
Recruiting
Conditions
Neuromuscular Diseases
Cerebral Palsy
Interventions
Other: Power wheelchair soccer
Registration Number
NCT06259643
Lead Sponsor
Université Catholique de Louvain
Brief Summary

This study is a prospective interventional study. It will be conducted at a single center with participants who have neuromotor impairments. The primary objective is to assess and measure the clinical and psychosocial effects of a season of power wheelchair soccer among its participants presenting with severe motor impairments due to neuromuscular lesion.

A maximum of twenty participants will be recruited and included in the same group. Data collection will be performed before, during, and after the wheelchair soccer season. The study will span the entire season, starting in November 2023 and ending in June 2024.

Clinical and psychosocial assessments will be conducted every 3 months. Each assessment session will last 2 hours per participant. Before and after the wheelchair soccer season matches, we will evaluate parameters related to the physical load of the sport. These evaluations will last 10 minutes per participant.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
20
Inclusion Criteria
  • Being a male or female between the ages of 12 and 50.
  • Presenting with severe motor impairments due to neuromotor and/or musculoskeletal impairment.
  • Using a power wheelchair in everyday life.
  • Being part of a power wheelchair soccer team.
  • Committing to participating in the 2023-2024 season of their sport within the team.
Exclusion Criteria
  • Practicing another adaptive sport outside of power wheelchair soccer in a regular way (once a week or more).

  • Occasionally practicing power wheelchair soccer (twice a month or less).

  • Presenting with severe cognitive impairments affecting understanding of instructions on how to answer questionnaires and undertake tests.

  • Presenting with contraindications towards the practice of an adaptive sport such as power wheelchair soccer.

    • Participating in another study at baseline.

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Power wheelchair soccerPower wheelchair soccersoccer game performed with a wheelchair
Primary Outcome Measures
NameTimeMethod
Social participationThroughout the entire study (an average of 8 months)

Social participation will be assessed using the Questionnaire of young people's participation.Scores range from 0 to 239, where a higher score displays greater social participation.

BalanceThroughout the entire study (an average of 8 months)

Balance will be measured using the function section of the Seated Postural Control measure. Scores range from 12 to 48, where a higher score is attributed to individuals with better postural control.

Strength of the upper-limbsThroughout the entire study (an average of 8 months)

Strength of the main muscle groups of the upper-limb will be measured using a Microfet 2 dynamometer.

Passive range of motion the upper-limbsThroughout the entire study (an average of 8 months)

Passive range of motion of the upper-limbs will be measured using a goniometer.

Hyperactivity of the musclesThroughout the entire study (an average of 8 months)

Hyperactivity of the muscles will be measured using the Penn Spasm Frequency Scale. Scores range from 0 to 4, where a higher score represents more frequent spasms and hyperactivity of the muscles.

Sensorimotor impairmentThroughout the entire study (an average of 8 months)

Sensorimotor impairment will be measured by the Fugl-Meyer assessment.

Quality of lifeThroughout the entire study (an average of 8 months)

Quality of life will be assessed using the KIDSCREEN 27 questionnaire. Scores range from 10 and 50, where 50 represents a very high health-related quality of life.

Autonomy during activities of daily lifeThroughout the entire study (an average of 8 months)

Autonomy during activities of daily life will be assessed using the Impact on participation and autonomy questionnaire. A participation score (range: 30-155) and a problem score (0-16) are produced by summing items in each scale. For both, a higher score represent poorer autonomy and more severe difficulty.

PainThroughout the entire study (an average of 8 months)

Pain perceived by the participants in their daily life will be measured using the PROMIS pain-pediatric Short Form V2 questionnaire. Scores range from 8 to 40, where a higher score displays more pain in everyday life.

Skills to manage and move power wheelchairThroughout the entire study (an average of 8 months)

Skills to manage and move power wheelchair will be assessed by the Wheelchair Skills Test Questionnaire version 4.2. Scores range from 0 to 100%, where a greater percentage represents better skills.

Secondary Outcome Measures
NameTimeMethod
Body temperatureThroughout the entire study (an average of 8 months)

Body temperature will be evaluated using a tympanic thermometer.

Blood oxygen saturationThroughout the entire study (an average of 8 months)

Blood oxygen saturation will be evaluated using a pulse oximeter.

Heart beat rateThroughout the entire study (an average of 8 months)

Heart beat rate will be evaluated using a heart rate monitor.

Blood pressureThroughout the entire study (an average of 8 months)

Blood pressure will be evaluated on the left upper-arm with a tensiometer. Both systolic and diastolic pressure will be recorded.

Trial Locations

Locations (1)

Neuromusculoskeletal Lab

🇧🇪

Brussels, Belgium

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