CanMove: A Physical Activity Program for Children With Cancer

Murdoch Childrens Research Institute

Status

Completed

Conditions

Pediatric Cancer

Treatments

Behavioral: Complex physical activity intervention

Study type

Interventional

Funder types

Other

Identifiers

NCT04483362

MurdochCRI

Details and patient eligibility

About

This study will evaluate a physical activity intervention for children during acute cancer treatment. The intervention aims to encourage children to participate in increased levels of physical activity and reduce the amount of time they spend engaged in sedentary activities. This study also aims to evaluate different ways of assessing physical function in order to determine the best outcome measure to use for children during acute cancer treatment.

Full description

All participants will receive the intervention which involves weekly sessions with a physiotherapist and the provision of an activity tracker. The sessions will aim to help motivate participants to be more physically active and identify barriers to physical activity in their environment. The activity tracker will be used to set a steps per day goal for the participant to achieve.

The intervention will be assessed for feasibility using aspects of the Bowen Framework. Under this framework the intervention will be evaluated according to different domains:

Acceptability: To what extent is a new idea, program, process or measure judged as suitable or satisfying
Demand: To what extent is a new idea, program, process, or measure likely to be used
Implementation: To what extent can a new program is successfully delivered to intended participants
Practicality: To what extent can the program can be carried out with intended participants using existing means, resources, and circumstances
Limited efficiency: Does the a new program show promise of being successful with the intended population

In order to find out the best way to assess physical function, participants will complete 5 different assessments. The results from these assessments will help to determine the best measure to use in this population.

Enrollment

21 patients

Sex

All

Ages

5 to 17 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Is between the ages of 5-17 years at the time of consent
Diagnosed (or relapsed) with cancer >4 weeks and <6 months at time of consent
Currently receiving cancer treatment at the Royal Children's Hospital
Has been an in-patient for >7 consecutive days at the time of consent
Provide a signed and dated informed consent form and/or has a legally acceptable representative capable of understanding the informed consent document and providing consent on the participant's behalf

Exclusion criteria

Deemed by the treating medical team as unsafe to participate
Child/adolescent unable to mobilise independent of clinical staff assistance, as classified by the research team at the time of consent (use of a gait aid or assistance from a primary carer/support person is accepted). For example, if a child/adolescent requires assistance from nursing staff or physiotherapist in order to walk, they will be excluded.
Child/adolescent unable to follow simple instructions
Suitable support person (18 years and over) not available to participate in continuous monitoring of daily steps in tandem with the child/adolescent
No suitable access to a device to sync with a Fitbit
Inability or unwillingness of participant or legally acceptable representative to give written informed consent.