TrialReader


SMART Project in Preventing Skin Cancer

NCT03177057 — Not applicable, Completed, 114 participants, Fox Chase Cancer Center

ClinicalTrials Daily  ·  Areas  ·  Conditions  ·  Drugs  ·  Sponsors  ·  

Self-Monitoring and Readiness Texting Project (SMART)

RegistryNCT03177057, acronym SMART
StatusCompleted
PhaseNot applicable
Study typeInterventional; randomized, parallel, masking: none, health services research
Enrollment114 (Actual)
SponsorFox Chase Cancer Center (Other); collaborators: National Cancer Institute (NCI)
ConditionsSkin Carcinoma
InterventionsCompliance Monitoring, Health Telemonitoring, Questionnaire Administration (Behavioral, other)
Datesstart 2013-04-23, primary completion 2014-07-30, completion 2014-12-31, first posted 2017-06-06, last updated 2018-08-01
Locations1 site in United States

Related Papers Related Patents Related Grants Related Experts
AI Assistant Save
All trials for Skin Carcinoma All trials of Compliance Monitoring All trials of Health Telemonitoring

-Summary

This pilot clinical trial studies how well Self Monitoring And Readiness Texting (SMART) project works in sun exposure and protection behaviors. Measuring how behavior tracking and individually tailored messages affect risk behaviors in patients with skin cancer may help doctors plan the best prevention plan and decrease national melanoma incidence and mortality.

Expand all sections  ·  Collapse all

+Detailed description

PRIMARY OBJECTIVES:

I. To test the effects of a behavior tracking and individually-tailored daily text message intervention on sun protection and exposure behaviors and to see if these techniques will be most effective in conjunction or separately.

SECONDARY OBJECTIVES:

I. To examine mediators in the effects of the intervention on safe sun behaviors, based on Fishbein?s Integrative Model.

OUTLINE: Patients are randomized to 1 of 4 study arms.

ARM I (SELF-MONITORING): Patients complete tanning and sun protection usage entries daily for 14 days.

ARM II (TEXT MESSAGES): Patients receive individualized text messages based on baseline assessment of tanning motives (appearance, enjoyment, social) daily for 14 days.

ARM III (COMBINED GROUP): Patients complete tanning and sun protection usage entries and also receive individualized text messages daily for 14 days.

ARM IV (CONTROL GROUP): Patients complete study assessments.

After completion of study, patients are followed up at 2 weeks.

+Arms and interventions

ArmTypeInterventionsDescription
Arm I (self-monitoring)ExperimentalBehavioral: Compliance Monitoring; Other: Questionnaire AdministrationARM I (SELF-MONITORING): Patients complete tanning and sun protection usage entries daily for 14 days.
Arm II (text messages)ExperimentalOther: Health Telemonitoring; Other: Questionnaire AdministrationARM II (TEXT MESSAGES): Patients receive individualized text messages based on baseline assessment of tanning motives (appearance, enjoyment, social) daily for 14 days.
Arm III (self-monitoring, text messages)ExperimentalBehavioral: Compliance Monitoring; Other: Health Telemonitoring; Other: Questionnaire AdministrationARM III (COMBINED GROUP): Patients complete tanning and sun protection usage entries and also receive individualized text messages daily for 14 days.
Arm IV (questionnaire administration)Sham comparatorOther: Questionnaire AdministrationARM IV (CONTROL GROUP): Patients complete study assessments.
  • Compliance Monitoring (Behavioral): Record behavior
  • Health Telemonitoring (Other): Receive health monitoring text messages
  • Questionnaire Administration (Other): Ancillary studies

+Outcome measures

Primary outcomes

  • Change in ultraviolet radiation (UV) exposure and sun protection behaviors based on behavior tracking and individually tailored daily text messages [Baseline to up to 2 weeks]: Multiple variable regression models will be performed to examine the effect of the intervention on the outcomes. All post-baseline outcomes will be used as dependent variables. The baseline scores, intervention group, and time of the assessment will be included. To account for the within subject correlation of the responses, we will fit the model using Generalized Estimating Equations assuming an autoregressive working correlation matrix for each subject. Any p-value from the pairwise comparison that is less than 0.05 will be considered worthy of further study.

Secondary outcomes

  • Mediators and moderators of the intervention on behavior [At 2 weeks]: Mediation will be assessed by examining indirect effects, with bootstrapped confidence intervals to be calculated around the mediated effects. For participants who use the self-monitoring app, hierarchical linear modeling will be used to examine associations between tanning and sun protection as they occur daily, and motives for doing so. Using lagged multi-level models, the within-person model allows for assessment of individual change in behavior over the two-week time period, as well as the effect of each day?s behavior on behavior occurring on subsequent days. The between-person model allo

+Eligibility

Sex: Female, ages: 18 Years to 29 Years

Inclusion Criteria:

* Women from the Philadelphia metropolitan area who own a mobile phone and who meet criteria for at least moderate risk of skin cancer based on a brief risk assessment tool

+Locations (1)

FacilityCityCountryStatus
Fox Chase Cancer CenterPhiladelphia, PennsylvaniaUnited States

+Investigators

+Funding

NIH grants: P30CA006927

My Notes