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Effect of Laughie on Pain Anxiety and Pain Level in Second-Degree Burn Patients (LA-PAP)

H

Hacettepe University

Status

Not yet enrolling

Conditions

Second Degree Burns
Burn

Treatments

Other: Laughie

Study type

Interventional

Funder types

Other

Identifiers

NCT07386821
TABED 2-25-1864

Details and patient eligibility

About

Burn injuries are traumatic conditions that seriously affect individuals' quality of life, both physically and psychologically. Second-degree burns, in particular, affect the superficial and/or deep layers of the dermis, causing intense pain and extensive tissue damage. Pain in burn patients is not only physical; it combines with emotional stress, fear, and uncertainty to increase anxiety levels.

This study is a parallel group-randomised controlled trial designed to evaluate the effects of the Laughie exercise, administered prior to dressing changes in individuals diagnosed with second-degree burns, on post-dressing pain anxiety levels and pain intensity.

Enrollment

88 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 18 years of age and over
  • Having a second degree burn
  • Arriving for the second dressing change on the unit
  • To agree to participate in the research

Exclusion criteria

  • In multiple burns, a burn degree other than the second degree on any part of the body
  • A maximum of 96 hours have elapsed since the burn injury
  • To have come to the dressing in repetitions other than the second dressing
  • Inability to tolerate the Laughie exercise

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

88 participants in 2 patient groups

Intervention Group
Experimental group
Description:
Laughie
Treatment:
Other: Laughie
Control Group
No Intervention group
Description:
Control: Second-degree burn patients. For patients presenting for their second dressing change, standard dressing change prosedures will be applied. The study procedure will include the following steps: (1) collection of descriptive characteristics; (2) assessment of pain severity and pain anxiety levels 5-10 minutes before the dressing change; (3) application of the dressing; (4) reassessment of pain severity and pain anxiety levels five minutes after the procedure.

Trial contacts and locations

1

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Central trial contact

Merve Akın, MD, Assoc. Prof.; Burcu Duluklu, PhD, Asst. Prof.

Data sourced from clinicaltrials.gov

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