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临床试验/NCT07418515
NCT07418515已完成不适用

Impact of Therapeutic Storytelling on Fear, Screen Time, and Parental Stress Among Hospitalized Children: A Randomized Controlled Trial

Karabuk University1 个研究点 分布在 1 个国家目标入组 44 人开始时间: 2024年6月1日最近更新:
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
44
试验地点
1
主要终点
The Scale Of Fear In Children Against Nursing Interventions And Used Materials

研究概览

简要总结

The goal of this clinical trial is to learn whether therapeutic story reading reduces fear levels, problematic media use, and parental stress in hospitalized preschool children. It will also examine the effectiveness of this intervention when integrated into routine nursing care.

The main questions it aims to answer are:

Does therapeutic story reading reduce children's fear of nursing interventions and medical materials?

Does therapeutic story reading reduce problematic media use in hospitalized children?

Does therapeutic story reading reduce parental stress levels?

Researchers will compare a therapeutic story reading intervention to routine care to determine whether the intervention improves psychological outcomes in hospitalized children and their parents.

Participants will:

Be randomly assigned to either the intervention group or the control group

Complete baseline assessments before the intervention

(Intervention group) Participate in therapeutic story reading sessions for three consecutive days

(Control group) Receive routine hospital care

Complete post-intervention assessments after the study period

Children's fear levels will be assessed using the Fear of Children Against Nursing Interventions and Used Materials Scale (FCANIM). Parental outcomes will be measured using the Problematic Media Use Measure (PMUM) and the Parental Stress Scale (PSS).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
4 Years 至 6 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Children aged 4-6 years
  • Able to speak and understand Turkish
  • Hospitalized in the pediatric ward for at least 3 days
  • No diagnosed cognitive impairment
  • Written informed consent provided by a parent or legal guardian to participate in the study

排除标准

  • Children who do not speak or understand Turkish
  • Hospital stay expected to be less than 3 days
  • Presence of diagnosed cognitive impairment or developmental disorder that would interfere with participation
  • Children whose parent or legal guardian does not provide informed consent
  • Children with a medical condition requiring intensive care or isolation precautions that would prevent participation in the intervention

研究组 & 干预措施

Storytelling group

Experimental

Participants in the intervention arm received a structured therapeutic story reading intervention during their hospitalization in the pediatric ward. The intervention was implemented on three consecutive days during the child's inpatient stay, at a time that did not interfere with medical treatment or nursing care, and was conducted in the child's hospital room.

One therapeutic storybook was read per day (three books in total). The intervention was primarily delivered by a pediatric nursing specialist researcher.

Three therapeutic storybooks specifically selected to positively influence the hospitalization experience were used:

"I Have a Fever" - aimed at helping children understand fever and related nursing interventions.

"From A to Z: Hospital (Interactive Alphabet)" - aimed at familiarizing children with hospital equipment and healthcare professionals.

"Sometimes It Happens: I Guess I Felt a Little" - aimed at helping children recognize and express fear related to hospitalization.

干预措施: Therapeutic Story Telling (Behavioral)

Routine care group

Other

Participants in the routine care arm received routine pediatric ward care without therapeutic story reading sessions.

干预措施: routine care (Other)

结局指标

主要结局

The Scale Of Fear In Children Against Nursing Interventions And Used Materials

时间窗: At baseline (prior to the intervention) and immediately after completion of the 3-day intervention period.

Fear levels are assessed using the Fear of Children Against Nursing Interventions and Used Materials Scale (FCANIM), a 18-item instrument developed to evaluate children's fear of nursing procedures and commonly used medical materials. The scale consists of two subdimensions: (1) fear of frequently encountered materials and (2) fear of less frequently encountered materials. Each item includes a visual representation of a nursing intervention or medical material (e.g., stethoscope, thermometer). Children rate their level of fear for each image using a five-point Likert-type scale illustrated with facial expressions representing increasing levels of fear. Total scores range from 18 to 90. Higher scores indicate higher levels of fear toward nursing interventions and medical materials, while lower scores indicate lower fear levels. The internal consistency of the scale is high, with Cronbach's alpha coefficients ranging from 0.89 to 0.93 for the subdimensions and 0.94 for the total scale.

Problematic Media Use Measure

时间窗: At baseline (prior to the intervention) and immediately after completion of the 3-day intervention period.

Problematic media use is assessed using the 9-item Problematic Media Use Scale - Short Form (PMUS-SF). The scale evaluates problematic use of screen-based media devices, including television, computers, tablets, and smartphones. Items are rated on a 5-point Likert scale based on the frequency of screen-use behaviors. The total score is calculated by summing the item scores and dividing by nine. Final scores range from 1 to 5. Higher scores indicate higher levels of problematic media use, whereas lower scores indicate lower levels of problematic media use. The original scale demonstrated high internal consistency (Cronbach's alpha = 0.92). In the present study, Cronbach's alpha was 0.78 at pre-test and 0.80 at post-test.

Parental Stress Scale

时间窗: At baseline (prior to the intervention) and immediately after completion of the 3-day intervention period.

Parental stress is assessed using the 16-item Parental Stress Scale (PSS). The scale consists of four subdimensions: parental stressors, loss of control, satisfaction, and rewards. Items are rated on a 5-point Likert-type scale. Total scores range from 16 to 80. Higher scores indicate higher levels of parental stress, whereas lower scores indicate lower levels of parental stress. In the Turkish validation study, Cronbach's alpha coefficients for the subscales ranged between 0.70 and 0.76, and 0.81 for the total scale score. In the present study, Cronbach's alpha was 0.73 at pre-test and 0.76 at post-test.

次要结局

未报告次要终点

研究者

发起方
Karabuk University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Yeliz Taşdelen

Assisstant professor

Karabuk University

研究点 (1)

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