Short-term Effects Kinesiology Tape on Sitting Postural Control in Moderate and Severe Cerebral Palsy (KT-SIT_CP)

May 31, 2024 updated by: University of Castilla-La Mancha
To analyze the short-term effect of kinesiology taping on sitting postural control in moderate and severe cerebral palsy

Study Overview

Study Type

Interventional

Enrollment (Actual)

12

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Toledo, Spain, 45006
        • Javier Merino Andrés

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

4 years to 14 years (Child)

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • age between 4 and 14 years
  • diagnosis of motor and cognitive disability
  • have prescribed physiotherapy treatment at school
  • acquisition of autonomous sitting
  • sign the consent informed

Exclusion Criteria:

  • presentation of an allergic reaction to tape
  • presentation of wounds in the area of application of the tape
  • having received botulinum toxin treatment in the last 6 months

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Non-Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Kinesiology taping
Apply a kinesiology taping on the abdominal muscles plus conventional physiotherapy
We used kinesiology taping in abdominal muscles
Active Comparator: Physiotherapy Group
Apply a conventional physiotherapy
We used conventional physiotherapy to comparate

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Posture and Postural Ability Scale - T0
Time Frame: pre-intervention
Posture and Postural Ability Scale pre-intervention (PPAS pre). Score from 0 to 7, and the higher the score, the better posture
pre-intervention
Posture and Postural Ability Scale - T1
Time Frame: at 10 days
Posture and Postural Ability Scale post-intervention (PPAS post). Score from 0 to 7, and the higher the score, the better posture
at 10 days
Segmental Assessment of Trunk Control - T0
Time Frame: pre-intervention
Segmental Assessment of Trunk Control pre-intervention (SATco pre). Score from 1 to 7, and the lower the score, the better balance
pre-intervention
Segmental Assessment of Trunk Control - T1
Time Frame: at 10 days
Segmental Assessment of Trunk Control post-intervention (SATco post).Score from 1 to 7, and the lower the score, the better balance
at 10 days

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Javier Merino Andrés, MSc, Researcher

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

March 15, 2020

Primary Completion (Actual)

July 15, 2020

Study Completion (Actual)

July 30, 2020

Study Registration Dates

First Submitted

July 21, 2021

First Submitted That Met QC Criteria

August 4, 2021

First Posted (Actual)

August 5, 2021

Study Record Updates

Last Update Posted (Actual)

June 3, 2024

Last Update Submitted That Met QC Criteria

May 31, 2024

Last Verified

May 1, 2024

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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