Trunk and Upper Extremities Program Effect in Decreasing Compensation Patterns in Unilateral Cerebral Palsy Children

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age8-16
SponsorFundacio Aspace Catalunya

About this trial

The goal of this clinical trial is to test the effectiveness of a trunk and upper extremities exercise program. The main questions it aims to answer are:

Whether the program decreases compensation patterns in unilateral cerebral palsy children Whether the program decreases pain in unilateral cerebral palsy children Whether the program improves bimanual ability in unilateral cerebral palsy children Participants will undertake and 8-week program exercise at home If there is a comparison group: Researchers will compare with the control group to see if this program decreases compensation patterns.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Unilateral cerebral palsy diagnostic

Level I or II of the Manual Ability Scale Classification

Disqualifiers

Have received any intervention with botulinum toxin or shock waves in the previous six months or have them scheduled during the intervention

Are undergoing treatment with intensive therapies.

To have known alteration in the hips

Have very serious attention or comprehension difficulties that prevent them from following instructions.

Trial design

Design model

Parallel

Treatments tested in this trial

  • TUPEX

    Other intervention

    This program contains exercises with their own body weight or with Thera-bands for gaining strength in their shoulder and trunk muscles. It contains some progression exercise if needed. Each session can last between 20 and 30 minutes. Children have to do each session three times a week during 8 weeks.

Treatment groups

40 Participants
are divided into 2 treatment groups
Group A: Standard groupNo intervention 0 interventions
Group B: TUPEX groupExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Rate of variance of the Compensation patterns

DeepLabCut (DLC) (Artificial Intelligence). Calculate the kinematic difference of the body marks during the activities

Time frame
8 weeks

Secondary outcomes

1

Intensity of pain

Face Pain Scale - Revised (FPS-R). The face marked is compared before and after the treatment. 0 is the minimum scores, meaning no pain, and 10 is the maximum score, meaning really severe pain.

Time frame
8 weeks
2

Location of pain

In the Body Diagram. The location of the pain is compared before and after the treatment

Time frame
8 weeks
3

Bimanual ability

Children Hand-Use Experience Questionaire 2.0 (CHEQ 2.0). Whether they are more capable of doing more bimanual activities or not. The maximum score in each question is 100 and the minimum is 0. 100 means children use their hands like the neurotypical children, and 0 means they can't use the affected hand at all.

Time frame
8 weeks

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Fundacio Aspace Catalunya

Lead sponsor

Universitat Internacional de Catalunya

Collaborator

This trial is not recruiting at the moment. You can still explore other options: