NCT06583668

Brief Summary

Aim: The aim of this study was to evaluate the effect of therapeutic story on pain, anxiety, fear and physiological parameters in children undergoing burn dressing. Methods: A randomised controlled trial was conducted between April 2023 and June 2024 with 60 patients who were admitted to the burn unit of a hospital in Istanbul and met the inclusion criteria. Patients in the story group (n=30) were listened to the digitised story during burn dressing, while patients in the control group (n=30) did not receive any intervention other than routine care. Data were collected using the Descriptive Characteristics Form, Child Anxiety Scale-Situation Scale, Child Fear Scale, Wong-Barker Pain Scale, Parental Satisfaction Scale (VAS) and Physiological Parameters Form.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
60

participants targeted

Target at P25-P50 for not_applicable pain

Timeline
Completed

Started Apr 2023

Typical duration for not_applicable pain

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

April 1, 2023

Completed
1.2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2024

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

July 1, 2024

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

August 27, 2024

Completed
8 days until next milestone

First Posted

Study publicly available on registry

September 4, 2024

Completed
Last Updated

September 19, 2024

Status Verified

September 1, 2024

Enrollment Period

1.2 years

First QC Date

August 27, 2024

Last Update Submit

September 5, 2024

Conditions

Keywords

AnxietyBurnChildPainFear

Outcome Measures

Primary Outcomes (3)

  • The effect of therapeutic history on pain

    Wong Barker Pain Scale The Facial Expressions Rating Scale (Wong Baker) consists of six facial expressions. The facial expressions are graded as 'No pain=0 points' and 'Unbearable pain=10 points'. It is a scale based on the child's self-report and is suitable for use in children aged 3-18 years. In this scale, pain scores are given according to the numerical values given to the faces. The lowest score is '1' and the highest score is '5'. As the score obtained from the scale increases, pain tolerance decreases and as the score decreases, tolerance increases. This scale was used before, during and after the burn dressing.

    15 month

  • The effect of therapeutic history on fear

    The scale is used to assess fear in children aged 4-10 years. The scale consists of five drawn facial expressions ranging from neutral expression (0=no anxiety) to frightened face (4=severe anxiety). This scale was used before, during and after the burn dressing.

    15 month

  • The effect of therapeutic history anxiety

    Child Anxiety Scale-Dispositional (CAS-D) Scale The Child Anxiety Scale-Dispositional (CAS-D) Scale aims to determine the anxiety levels of children aged 4-10 years. The CAS-D is shaped like a thermometer with a light bulb at the bottom and horizontal lines with intervals going upwards. In order to measure the state anxiety level, the child is asked to mark how he/she feels 'at the moment'. A transparent metre is placed over the child's rating on which ½ point increments are marked, then the ½ point increment is rounded up to the nearest number. The score can range from 0 to 10.It is determined that as the score value increases, the anxiety level increases, and as the score value decreases, the anxiety level decreases. This scale was used before, during and after the burn dressing.

    15 month

Secondary Outcomes (4)

  • The effect of the therapeutic story applied to children on parents' anxiety levels

    15 month

  • The effect of therapeutic history on blood pressure/systolic -diastolic

    15 month

  • The effect of therapeutic history on pulse rate

    15 month

  • The effect of therapeutic history on saturation levels

    15 month

Study Arms (2)

Experimental: Therapeutic Story group

EXPERIMENTAL

I. Assessment:Before the burn dressing II. Assessment: During burn dressing II. Assessment: After burn dressing

Other: Therapeutic Story

Standard care

NO INTERVENTION

I. Assessment:Before the burn dressing II. Assessment: During burn dressing II. Assessment: After burn dressing

Interventions

Listening and watching the therapeutic story in digital media

Experimental: Therapeutic Story group

Eligibility Criteria

Age3 Years - 6 Years
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17)

You may qualify if:

  • \- To be between 3-6 years old,
  • Consideration of the first dressing of the child in the burn centre
  • nd degree superficial and deep burns (2nd degree burns requiring hospital treatment and high pain level)
  • Percentage of burns below 10 per cent (light sedation for children with burn injuries above 10 per cent)
  • Not having any chronic disease other than burns
  • The child's willingness to participate in the research
  • It is the absence of mental, communication problems and visual impairment.

You may not qualify if:

  • The child's dressing has been done in a burn center before
  • Presence of 1st and 3rd degree burn areas
  • Burn percentage is over 10%

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Istanbul- City Hospital

Istanbul, Turkey (Türkiye)

Location

Related Publications (4)

  • Hawker GA, Mian S, Kendzerska T, French M. Measures of adult pain: Visual Analog Scale for Pain (VAS Pain), Numeric Rating Scale for Pain (NRS Pain), McGill Pain Questionnaire (MPQ), Short-Form McGill Pain Questionnaire (SF-MPQ), Chronic Pain Grade Scale (CPGS), Short Form-36 Bodily Pain Scale (SF-36 BPS), and Measure of Intermittent and Constant Osteoarthritis Pain (ICOAP). Arthritis Care Res (Hoboken). 2011 Nov;63 Suppl 11:S240-52. doi: 10.1002/acr.20543. No abstract available.

    PMID: 22588748BACKGROUND
  • Farzan R, Parvizi A, Haddadi S, Sadeh Tabarian M, Jamshidbeigi A, Samidoust P, Ghorbani Vajargah P, Mollaei A, Takasi P, Karkhah S, Firooz M, Hosseini SJ. Effects of non-pharmacological interventions on pain intensity of children with burns: A systematic review and meta-analysis. Int Wound J. 2023 Sep;20(7):2898-2913. doi: 10.1111/iwj.14134. Epub 2023 Mar 1.

    PMID: 36859758BACKGROUND
  • Chester SJ, Stockton K, De Young A, Kipping B, Tyack Z, Griffin B, Chester RL, Kimble RM. Effectiveness of medical hypnosis for pain reduction and faster wound healing in pediatric acute burn injury: study protocol for a randomized controlled trial. Trials. 2016 Apr 29;17(1):223. doi: 10.1186/s13063-016-1346-9.

    PMID: 27129580BACKGROUND
  • Jeffs D, Dorman D, Brown S, Files A, Graves T, Kirk E, Meredith-Neve S, Sanders J, White B, Swearingen CJ. Effect of virtual reality on adolescent pain during burn wound care. J Burn Care Res. 2014 Sep-Oct;35(5):395-408. doi: 10.1097/BCR.0000000000000019.

    PMID: 24823326BACKGROUND

MeSH Terms

Conditions

PainBurnsAnxiety Disorders

Condition Hierarchy (Ancestors)

Neurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and SymptomsWounds and InjuriesMental Disorders

Study Officials

  • Niran ÇOBAN, Dr

    Okan University

    STUDY DIRECTOR
  • Niran ÇOBAN, Dr

    https://www.okan.edu.tr/

    STUDY DIRECTOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Asst.Prof.Dr.

Study Record Dates

First Submitted

August 27, 2024

First Posted

September 4, 2024

Study Start

April 1, 2023

Primary Completion

June 1, 2024

Study Completion

July 1, 2024

Last Updated

September 19, 2024

Record last verified: 2024-09

Data Sharing

IPD Sharing
Will not share

Locations