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Effectiveness of an Adventure-based Training Programme

Effectiveness of an Adventure-based Training Programme in Promoting the Psychological Well-being of Primary School Children

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02517450
Enrollment
120
Registered
2015-08-07
Start date
2010-04-30
Completion date
2011-10-31
Last updated
2015-08-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy

Keywords

Subjects

Brief summary

This study tested the effectiveness of an adventure-based training programme in promoting the psychological well-being of primary schoolchildren. A randomised controlled trial was conducted, with 56 primary school pupils randomly assigned to the experimental group participating in the adventure-based training programme and 64 to the attention placebo control group.

Interventions

BEHAVIORALan adventure-based training programme

The programme consisted of five education sessions (around 75 minutes each) and a day's adventure-based training camp at the end of the academic year

OTHERa placebo control programme

Subjects in the control group were invited to attend five 75-minute sessions of leisure activities, organised by a community centre, which included a cartoon film show, handicraft workshops, a health talk on the prevention of influenza and age-appropriate physical leisure activities, such as table tennis, badminton, chess and Chinese billiards. Additionally, they were invited to join a day visit to Hong Kong Ocean Park at the end of the academic year.

Sponsors

The University of Hong Kong
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
9 Years to 14 Years
Healthy volunteers
Yes

Inclusion criteria

* Hong Kong Chinese primary pupils from forms 5 and 6 of two schools were invited to participate in the study.

Exclusion criteria

* those with a chronic illness or identified cognitive and learning problems were excluded.

Design outcomes

Primary

MeasureTime frameDescription
The Center for Epidemiologic Studies Depression Scale for Children at baselinebaselinebaseline depressive symptoms
change of The Center for Epidemiologic Studies Depression Scale for Children at 9 months from baseline9 monthsdepressive symptoms after the last intervention session
change of The Center for Epidemiologic Studies Depression Scale for Children at 12 months from baseline12 monthsdepressive symptoms after 3 months from the last intervention session

Secondary

MeasureTime frameDescription
The Rosenberg Self-esteem Scale at baselinebaselinebaseline self-esteem
change of The Rosenberg Self-esteem Scale at 9 month from baseline9 monthsself-esteem after the last intervention session
change of The Rosenberg Self-esteem Scale at 12 month from baseline12 monthsself-esteem after 3 months from the last intervention session
The Chinese version of the State Anxiety Scale for Children at baselinebaselinebaseline anxiety level
change of The Pediatric Quality of Life Inventory Generic at 9 months from baseline9 monthsquality of life after the last intervention session
change of The Pediatric Quality of Life Inventory Generic at 12 months from baseline12 monthsquality of life after 3 months from the last intervention session
The Pediatric Quality of Life Inventory Generic at baselinebaselinebaseline quality of life
change of The Chinese version of the State Anxiety Scale for Children at 9 months from baseline9 monthsanxiety level after the last intervention session
change of The Chinese version of the State Anxiety Scale for Children at 12 months from baseline12 monthsanxiety level after 3 months from the last intervention session

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026