Maternal Pain Catastrophizing Score is Related With Children's Postoperative Circumcision Pain

Sponsor
Samsun University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05950126
Collaborator
(none)
197
1
16.6
11.9

Study Details

Study Description

Brief Summary

The aim of this study was to evaluate the relation of maternal pain catastrophizing score with child's who underwent circumcision postoperative pain. A cross-sectional study and this study was performed at the Samsun University, Samsun Training and Research Hospital, Samsun, Türkiye. The mothers were divided into low pain catastrophizing (Group 1) and high pain catastrophizing (Group 2) group. Children's postoperative pain intensity was measured using the visual analog scale (VAS) and a faces pain scale (FPS).

Condition or Disease Intervention/Treatment Phase
  • Other: pain catastrophizing scala

Detailed Description

Now, the study is continuing.

Study Design

Study Type:
Observational
Anticipated Enrollment :
197 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Is Pain Perception Communicated Through Mothers? Maternal Pain Catastrophizing Score is Related With Children's Postoperative Circumcision Pain
Actual Study Start Date :
Apr 1, 2022
Anticipated Primary Completion Date :
Aug 1, 2023
Anticipated Study Completion Date :
Aug 20, 2023

Arms and Interventions

Arm Intervention/Treatment
Group 1

low pain catastrophizing score in mother

Other: pain catastrophizing scala
The PCS, a 13-item self-report inventory used to determine the extent to which individuals catastrophize in response to pain, was developed. Total possible scores range from 0 to 52, with higher scores indicating negative results. The Turkish version was tested for reliability and validity and the Cronbach alpha coefficient was measured at 0.90. PCS scores of 16 or lower are regarded as normal, and scores of 17 or above as high.

Group 2

high pain catastrophizing score in mother

Other: pain catastrophizing scala
The PCS, a 13-item self-report inventory used to determine the extent to which individuals catastrophize in response to pain, was developed. Total possible scores range from 0 to 52, with higher scores indicating negative results. The Turkish version was tested for reliability and validity and the Cronbach alpha coefficient was measured at 0.90. PCS scores of 16 or lower are regarded as normal, and scores of 17 or above as high.

Outcome Measures

Primary Outcome Measures

  1. PCS, mother, and child [18 month]

    Authors will be investigated the relationship between maternal pain catastrophizing score levels and the postoperative pain experienced by the child. Empathy towards pain is necessary to notice, understand, and respond to another person's pain. Children develop empathy towards pain over time, which may be related to social learning. Pain Catastrophizing scale (PCS): The PCS is a self-assessment questionnaire to examine catastrophizing in clinical and nonclinical populations. The PCS consists of 13 statements containing a number of thoughts and feelings one may experience when having pain. The items are divided into the categories of rumination, magnification and helplessness, with each item scored on a 5-point scale, from 0 (not at all) to 4 (always), people are asked to rate how often they experience the mentioned thoughts and feelings when they are in pain. The overall score has a range of 0-52.

Eligibility Criteria

Criteria

Ages Eligible for Study:
5 Years to 12 Years
Sexes Eligible for Study:
Male
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Age 5-12 years,

  • Being operated under general anesthesia.

Exclusion Criteria:
  • Children without biological mothers, or with a parent other than the mother,

  • Children aged under five or over 12,

  • History of previous surgery,

  • Being operated under regional anesthesia,

  • Use of analgesic, antiepileptic, or sedative medications, and

  • Other procedures being performed in addition to circumcision (such as herniorrhaphy, tonsillectomy, orchiopexy, and appendectomy).

Contacts and Locations

Locations

Site City State Country Postal Code
1 Samsun University Samsun Turkey 55090

Sponsors and Collaborators

  • Samsun University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

Responsible Party:
Sevda Akdeniz,MD, Principal investigator, Samsun University
ClinicalTrials.gov Identifier:
NCT05950126
Other Study ID Numbers:
  • B.30.2.ODM.0.20.08/80-165
First Posted:
Jul 18, 2023
Last Update Posted:
Jul 19, 2023
Last Verified:
Jul 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Sevda Akdeniz,MD, Principal investigator, Samsun University

Study Results

No Results Posted as of Jul 19, 2023