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The Primary Goal is to conduct a 5-10 week randomized controlled trial (RCT) of the Fitbit Flex, a popular, affordable, wearable physical activity tracking device, and the Fitbit mHealth app. The target population will be childhood cancer survivors 14-18 years old recruited from Seattle Children's Hospital. For the intervention group, peer influences will be engaged via a private, social network (e.g. a Facebook group) customized for survivors. Measurements will be completed (1) at baseline, prior to randomization, and (2) during the final week of the intervention period (follow-up measure). This study will provide initial proof of concept and allow for further customization of the intervention for childhood cancer survivors in anticipation of a future, larger proposal to study physical activity and related outcomes over a multi-year period.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Fitbit + Facebook | Experimental | Participants will use the Fitbit device and join the Facebook group. |
|
| Usual care control | No Intervention | No intervention provided. |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Fitbit | Behavioral | Participants will use the FitBit device to track their physical activity |
|
| Measure | Description | Time Frame |
|---|---|---|
| Post-intervention physical activity (measured by accelerometers) | up to week 10 |
| Measure | Description | Time Frame |
|---|---|---|
| Post-intervention health related quality of life (measured by questionnaire) | up to week 10 |
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Inclusion Criteria:
Exclusion Criteria:
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Seattle Children's Research Institute | Seattle | Washington | 98145-5005 | United States |
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| ID | Term |
|---|---|
| D009043 | Motor Activity |
| ID | Term |
|---|---|
| D001519 | Behavior |
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| Facebook group | Behavioral | Participants will receive and post messages and receive badges on the Facebook group |
|