The Effect of Cognitive-Behavioral Intervention Package on Procedural Pain and Anxiety in Children

Aynur Aytekin Ozdemir

Status: Completed

Conditions: Procedural Anxiety; Procedural Pain

Treatments: Behavioral: Cognitive-Behavioral Interventions Package

Study type: Interventional

Funder types: Other

Identifiers

NCT06018909

2018-3/20

Details and patient eligibility

About

This study investigated the effect of cognitive-behavioral interventions package (CBIP) on pain and anxiety related to peripheral venous cannulation (PVC) in children aged 7-12 years.

Full description

The International Guide to Pediatric Anesthesia (Good Practice in Postoperative and Procedural Pain) recommends pharmacological and nonpharmacological methods to effectively manage and prevent acute procedural pain in children. Nonpharmacological methods alone or in combination with pharmacological methods help reduce pain, and therefore, have become popular especially in recent years. For pain management, nonpharmacological methods are easy to use, and cost- and time-effective methods with no side effects. Studies have evaluated a large number of pharmacological and nonpharmacological interventions for procedural pain management in children. However, most of those interventions are not used by healthcare professionals because they are expensive, time-consuming or hard to use. Therefore, easy-to-use, practical, non-invasive, cost-effective, and reusable nonpharmacological methods can be used especially in acute settings. Cognitive-behavioral interventions, one of the non-pharmacological methods used to minimize pain and anxiety related to painful medical procedures in children are promising.

Enrollment: 80 patients

Sex: All

Ages: 7 to 12 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• being between the ages of 7 to 12 years
• be literate
• requiring peripheral venous cannulation procedure

Exclusion criteria

• had chronic diseases
• had neuro-developmentally delayed
• had visual, audio, or speech impairments
• were hospital stay for treatment in the past three years
• had a history of sedative, analgesic or narcotic use within 24 hours before procedure

Trial design

Primary purpose: Supportive Care

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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80 participants in 2 patient groups

Cognitive-Behavioral Interventions Package Group

Experimental group

Description:

Participants received CBIP. CBIP included procedural preparation and information, distraction, suggestions, parent training and positive reinforcement.

Treatment:

Behavioral: Cognitive-Behavioral Interventions Package

Control

No Intervention group

Description:

The control group received the routine peripheral venous cannulation procedure.