Skip to content

Dyadic Physical Activity Intervention for Children Undergoing Cancer Treatment

Dyadic-based Physical Activity Intervention for Children Who Are Undergoing Cancer Treatment: A Randomized Controlled Trial

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07737418
Acronym
DYAD-PA
Enrollment
198
Registered
2026-07-30
Start date
2027-01-01
Completion date
2030-01-01
Last updated
2026-07-31

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

Conditions

Leukemia, Physical Inactivity

Keywords

Leukemia, Physical Activity, Self-Efficacy, Parent-Child Dyad, Quality of Life, Randomized Controlled Trial, Maintenance Therapy, Under treatment, Exercise, Dyadic intervention, Pediatric oncology

Brief summary

The goal of this study is to learn if a parent-child dyadic physical activity (PA) intervention works to improve physical activity levels in children with leukaemia. It will also learn about the intervention's effects on children's self-confidence in doing physical activity and their quality of life. The main questions it aims to answer are: Does the dyadic PA intervention increase the amount of physical activity children do, compared with an individual PA intervention or usual care? Does the dyadic PA intervention improve children's confidence in doing physical activity and their overall quality of life? What is the cost-effectiveness of the dyadic intervention relative to the individual intervention and psychological support control group? Researchers will compare three groups: children and parents doing physical activity together (dyadic intervention), children doing physical activity individually (individual intervention), and children receiving psychological support sessions only (control group), to see if involving parents makes a difference. Participants will: Attend weekly sessions for 3 months (12 sessions total) Wear an activity tracker for 7 days and complete questionnaires at 5 different time points over 12 months Some participants will also be invited to take part in an interview about their experience

Interventions

Children receive the same structured 12-session, weekly physical activity intervention as the dyadic group, delivered over 3 months by a trained Research Assistant, without parental participation. Exercise intensity is individually tailored to each child.

BEHAVIORALPsychological Support

Children receive 12 weekly sessions of simple psychological support over 3 months, delivered by a trained Research Assistant, without a physical activity component.

BEHAVIORALDyadic Physical Activity Intervention

Parent-child dyads receive a structured physical activity intervention delivered by a trained Research Assistant over 12 weekly sessions across 3 months. Parents perform the physical activity together with their child in each session. Exercise intensity is individually tailored to each child.

Sponsors

The Hong Kong Polytechnic University
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Age
9 Years to 18 Years
Healthy volunteers
No

Inclusion criteria

* Children aged 9-18 years old * Diagnosed with leukaemia * Currently undergoing maintenance therapy * Have a parent willing to participate in the study * Both the child and participating parent speak Cantonese and read Chinese

Exclusion criteria

* Children under palliative care with evidence of cancer recurrence or second malignancies * Children with medical contraindications for PA, such as thrombosis, as documented by physicians * Children or parents with physical impairment or cognitive and learning problems (identified from medical records) * Participants in the team's other interventional studies

Design outcomes

Primary

MeasureTime frameDescription
Physical Activity LevelBaseline and 12 months(T4)Children's physical activity levels will be objectively measured using ActiGraph GT3X accelerometers, worn for 7 consecutive days at each assessment timepoint. The primary outcome is the minutes engaged in moderate-to-vigorous physical activity (MVPA).

Secondary

MeasureTime frameDescription
Self-Reported Physical Activity LevelBaseline, 3 months (T1), 6 months (T2), 9 months (T3), and 12 months (T4)Children's self-reported PA levels measured using the Chinese University of Hong Kong: Physical Activity Rating for Children and Youth, an 11-point scale (0-10) asking children to self-rate their PA levels in the past 7 days, from 0 (no exercise at all) to 10 (vigorous exercise on most days).
Health-Related Quality of Life Score (EQ-5D-Y-5L)Baseline, 3 months (T1), 6 months (T2), 9 months (T3), and 12 months (T4)Children's health-related quality of life will be measured using the EQ-5D-Y-5L. It includes a descriptive system covering five health dimensions, each scored from 1 to 5, with higher scores indicating worse outcomes, and the EQ visual analogue scale , scored from 0 to 100, with higher scores indicating better outcomes.
Physical Activity Self-Efficacy ScoreBaseline, 3 months (T1), 6 months (T2), 9 months (T3), and 12 months (T4)Children's physical activity self-efficacy will be assessed using the five-item Physical Activity Self-Efficacy Scale. Each item is rated on a three-point Likert scale. Total scores range from 5 to 15, with higher scores indicating greater physical activity self-efficacy.

Contacts

CONTACTKa Wai Katherine LAM
kw-katherine.lam@polyu.edu.hk+852 27666420

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 1, 2026