Skip to main content
Clinical Trials/NCT04883489
NCT04883489
Completed
Not Applicable

Clinical Classification of Musculoskeletal Pain in Caregivers for Children With Cerebral Palsy

Kutahya Health Sciences University1 site in 1 country60 target enrollmentMay 15, 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Chronic Pain
Sponsor
Kutahya Health Sciences University
Enrollment
60
Locations
1
Primary Endpoint
Numeric Pain Rating Scale
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

The care of children with Cerebral Palsy is a process that continues for many years. Individuals who take care of them experience musculoskeletal pain due to the difficulties they experience and face pain that becomes chronic over time. For individuals who take care of children with CP, determining the types of chronic pain is important in order to clarify the classification criteria and for individuals to reach better living standards by tailoring the treatments they will receive. Therefore, the aim of the study is to determine the types of chronic pain in caregivers for children with cerebral palsy.

Registry
clinicaltrials.gov
Start Date
May 15, 2021
End Date
January 1, 2022
Last Updated
3 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Kutahya Health Sciences University
Responsible Party
Principal Investigator
Principal Investigator

Ismail Saracoglu

Principal Investigator

Kutahya Health Sciences University

Eligibility Criteria

Inclusion Criteria

  • Having musculoskeletal pain complaints for the last 6 months or more
  • experienced musculoskeletal pain or a sensitive disorder (like numbness, tingling, etc.) anywhere in body for which they stated a minimum score of 2 on a numeric pain rating scale
  • pain that lasts at least 6 months
  • To provide the documented diagnosis of Cerebral palsy of the child in the care of the participants.

Exclusion Criteria

  • Having severe psychological illness
  • Having a cognitive dysfunction
  • Not participating in the assessment or submitting incomplete answers for questionnaires

Outcomes

Primary Outcomes

Numeric Pain Rating Scale

Time Frame: 1 minute

The NPRS was used to assess the participants' pain levels. In the NPRS, patients are asked to verbally rate the severity of their pain on a scale. The scale is composed of 0 (no pain at all) to 10 (worst imaginable pain).

Margolis Pain Diagram

Time Frame: 5 minute

The Margolis Pain Diagram, consists of a dorsal and a ventral drawing body, is used to assess the location and distribution of the pain. Participants will ask to point out the place where they experience pain during the preceding 4 weeks for at least 24 hours

Central Sensitization Inventory

Time Frame: 10 minute

The Central Sensitization Inventory (CSI) aims to evaluate symptoms thought to be associated with nociplastic pain. The CSI consists 25 items exploring emotional and somatic disorders associated with CS. Each response is scored from 0 to 4, yielding a total score of 0 to 100. A score of 40 or higher on the CSI means the presence of nociplastic pain.

Short Form 36

Time Frame: 10 minute

The Short Form-36 (SF-36) is widely used to measurement of health related quality of life (HRQoL) questionnaire. SF-36 is a 36-item generic self-administered instrument consisting of 8 subscales related to various aspects of HRQoL: physical functioning, physical role, bodily pain, general health, vitality, social functioning, emotional role, and mental health. The 8 subscales are scored from 0 to 100, with higher scores indicating better health status.

Secondary Outcomes

  • Quantitative sensory test(10 minute)

Study Sites (1)

Loading locations...

Similar Trials