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Clinical Trials in China / NCT06813625
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Shared Book Reading to Promote Mental Well-being Among Young People with and Without Down's Syndrome

NCT06813625 · tracked via the Priya Life Science China tracker
Sponsor
University of Macau
Phase
Not applicable
Started
2025-02-08
Last updated
2025-02-07

Condition(s) studied

Down Syndrome

Investigational drug(s) / intervention(s)

Shared book reading intervention

Shared book reading intervention: The intervention involved us pairing each teen DS with a college student to form a duo. Each group consists of one person with DS and at least one college student who will work together throughout the shared reading intervention. A weekly event hosted by a graduate student. It begins with ice-breaking activities such as color and music games to promote social interaction between participants. After the game, participants chose from a selection of 20 books suitable for different age groups. They can choose their own reading method, such as reading aloud or assigning roles, and are encouraged to share experiences in their own duos or in a large group of multiple duos. The session ends with a sharing and reflection activity where participants can discuss what they have read and plan for the next session.

Study summary

Abstract Background: With the progress of society and the deepening of people's understanding of Down syndrome (DS), research has shifted focus on how to improve the quality of life and education for young people with DS. This study shall pilot a shared book reading intervention to test for potential benefit and feasibility.

Methods: This study is an 8 weeks long pilot dyadic randomized controlled trial (RCT) comparing a shared book reading intervention to a minimal activity control, this study will then continue for 12 months as a single arm cohort study. Young people with DS and university undergraduate students will be recruited and formed into dyads then randomized to either intervention or control. The shared book reading activity will include partnering young people with DS and university students together for a weekly, 1-hour shared book reading session. The control group will be supplied with three books they can read in their free time during 8 weeks. The primary outcomes included young people with DS health-related quality of life measured using the Children's Quality of Life Scale (PedsQL4.0). Secondary outcomes include mental well-being in university students using the Engagement, Perseverance, Optimism, Connectedness, and Happiness scale (EPOCH). Measurements will be made at baseline (T0) and 8-week (T1). After 8 weeks all participants will be offered to continue in the study where all participants will join the shared book reading weekly intervention and outcomes measures will be made at 6-month (T2), and 12-month (T3) follow-up. Mixed linear regression models shall be conducted comparing intervention and control group at 8 weeks. At 6-months and 12-months follow-up change scores from baseline will be analyzed to test for potential long-term effect.

Anticipated results: If our pilot study can show that shared book reading activities for people with DS can be of benefit and feasible, this can lead to a fully powered randomized controlled trial.

Eligibility

Sex
ALL
Min age
2 Years
Max age
35 Years
Healthy volunteers
Accepted
Inclusion Criteria for Participants with Down Syndrome (DS): * Clinical diagnosis of Down Syndrome (DS). * Aged 2 years or older. * Able to participate in the intervention and study evaluation independently or with the support of caregivers or family members. Inclusion Criteria for University of Macau (UM) Students: * Aged 18 years or older. * Able to read and understand books in English or Chinese. * Able to communicate in English, Mandarin, or Cantonese. * Do not have severe visual or reading disabilities that may affect reading ability. Exclusion Criteria: -Have severe visual or reading disabilities.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
University of Macau Macau China

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06813625 on ClinicalTrials.gov ↗ ← All trials in China