MedPath

Narrative-based Card Game in Improving Spiritual Well-being Among Chinese Childhood Cancer Patients

Not Applicable
Not yet recruiting
Conditions
Pediatric Cancer
Interventions
Behavioral: Narrative-based card game
Registration Number
NCT05639062
Lead Sponsor
The Hong Kong Polytechnic University
Brief Summary

Cancer as a life-threatening disease can trigger children's unique spiritual needs. Unmet spiritual needs can cause low level of spiritual well-being, which is a central component for the overall quality of life (QoL) of cancer patients and was inversely associated with depressive symptoms, anxiety and a low level of hope. However, there has been no intervention focused on improving spiritual well-being among childhood cancer patients. Evidence from adult cancer patients suggests that narrative intervention can effectively address spiritual needs and improve spiritual well-being, while playing card game can combine an emotionally sensitive topic with an enjoyable activity, providing insight into the development of narrative-based card games for childhood cancer patients. The first objective of this pilot study is to assess the feasibility of narrative-based card game among Chinese childhood cancer patients. The second objective is to evaluate the preliminary effects of narrative-based card game intervention on spiritual well-being, hope, anxiety, depressive symptoms, and QoL of childhood cancer patients at postintervention and at 1-, and 3-month follow-up postintervention.

Detailed Description

A pilot randomized controlled trial will be carried out. A convenience sample of 60 children with cancer will be recruited. Subjects who are randomized into the experimental group which will participate the narrative-based card game or into the control group which will play a PUKE card game only for entertainment purpose, that mimics the time and attention of the intervention. Feasibility measures (i.e., the eligibility rate, consent rate, randomization rate etc.) will be collected immediately after the completion of the intervention. Also, all subjects will be asked to complete structured questionnaires to assess their spiritual well-being, hope, anxiety, depressive symptoms, and QoL at postintervention and at 1-, and 3-month follow-up postintervention.

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
60
Inclusion Criteria

(1) age 12-17 old (2) diagnosed with any type of cancer and currently undergoing active treatment (3) knowing about their cancer diagnosis, and (4) able to communicate with Chinese.

Exclusion Criteria

(1) those with identified cognitive and/or behavioural problems which affected their verbal communication; (2) those with advanced cancer, including nonresponsive to treatment, stage IV solid tumor that had recurred or progressed as defined, or physician estimated poor prognosis of <60%.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Narrative-based card gameNarrative-based card game-
Primary Outcome Measures
NameTimeMethod
Randomization ratebaseline

The number of participants who are randomized divided by the number of consenting children

Consent ratebaseline

The number of eligible childhood cancer patients who agree to participate divided by the number of eligible childhood cancer patients

Attendance ratepost-intervention

The number of participants in the experimental group who complete the intervention divided by the number of participants randomized into the group

Retention ratepost-intervention, and 1-month, 3- month follow ups

The number of participants who remain in the study divided by the number of participants randomized. Retention rate will be calculated at baseline and follow ups.

The length of recruitmentbaseline

The time used for subject recruitment

Missing datapost-intervention, 1-month, 3- month follow ups

The percentage of missing data.

Adverse eventspost-intervention, 1-month, 3-month follow ups

Unfavorable or unintended events during the study period that were not present at baseline or appear to have worsened since baseline.

Eligibility ratebaseline

The number of eligible childhood cancer patients divided by the number of childhood cancer patients screened prior to eligibility assessment

Completion ratepost-intervention, and 1-month, 3-month follow ups

The number of participants who complete the questionnaire divided by the number of questionnaires distributed.

Secondary Outcome Measures
NameTimeMethod
The Chinese version of adapted Functional Assessment of Chronic Illness Therapy Spiritual Well-being Scale at 3 months follow-upat 3-months follow-up

Assessing the spiritual well-being of participants, the score for the Chinese version of adapted Functional Assessment of Chronic Illness Therapy Spiritual Well-being Scale is 0-60, with higher scaores indicating higher spiritual well-being

Trial Locations

Locations (1)

Hong Kong Polytechnic University

🇭🇰

Hong Kong, Hong Kong

© Copyright 2025. All Rights Reserved by MedPath