Internet-based Intervention for Skin Self-Examination in Participants With Increased Risk for Melanoma
Study Details
Study Description
Brief Summary
This trial studies an internet-based intervention for skin self-examination (SSE) in participants at increased risk for melanoma. Early detection of suspicious growths on the skin can be done by performing regular SSE checks. Using an internet-based intervention, such as mySmartCheck, may help to promote regular, thorough checks on the skin in individuals at increased risk for melanoma.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
N/A |
Detailed Description
PRIMARY OBJECTIVES:
- To evaluate the impact of mySmartCheck versus usual care on skin-self-examination (SSE) behaviors among individuals at increased risk for developing melanoma.
SECONDARY OBJECTIVES:
-
To evaluate the impact of mySmartCheck versus usual care on patients barriers and benefits to conducting SSE, SSE self-efficacy (confidence), level of worry about developing melanoma, and number of health care consultations (visits, telephone calls, and emails).
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To evaluate whether mySmartCheck effects are moderated by the patient's Total Body Photography (TBP) status.
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To identify barriers and facilitators to using mySmartCheck.
OUTLINE:
PHASE I: Participants complete a telephone based usability testing of the online program. Participants complete between 1-5 user testing sessions of the mySmartCheck program (about 45-60 minutes per session) to provide feedback on acceptability, satisfaction, comprehension, and usability.
PHASE II: Participants are randomized to 1 of 2 groups. Both the intervention and control group complete a baseline survey as well as a 13 weeks post-baseline survey.
GROUP I: After completing the baseline survey, participants receive access to the mySmartCheck program, and continue to receive standard of care. Participants are asked to complete another survey 13 weeks post-baseline.
GROUP II: After completing the baseline survey, participants receive standard of care. Participants are asked to complete another survey 13 weeks post-baseline.
Study duration is 13 weeks for all participants.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Phase I (user testing) Participants complete telephone-based usability testing of the online program. Participants complete between 1-5 user testing sessions of the mySmartCheck program (about 45-60 minutes per session) to provide feedback on acceptability, satisfaction, comprehension, and usability. |
Behavioral: mySmartCheck
Receive access to mySmartcheck program
|
| Experimental: Phase II Group I (mySmartCheck) Participants are asked to complete a baseline survey. After completing the baseline survey, participants receive access to mySmartCheck program, and continue to receive standard of care. Participants are asked to complete another survey 13 weeks post-baseline. |
Other: Best Practice
Receive standard of care
Other Names:
Other: Survey Administration
Ancillary studies
|
| Experimental: Phase II Group II (standard of care) Participants are asked to complete a baseline survey. After completing the baseline survey, participants receive standard of care. Participants are asked to complete another survey 13 weeks post-baseline. |
Other: Best Practice
Receive standard of care
Other Names:
Other: Survey Administration
Ancillary studies
|
Outcome Measures
Primary Outcome Measures
- Performance of thorough skin-self examination (SSE) [Up to 13 weeks]
Thorough SSE is defined as thoroughly examining each area of the body during the most recent SSE skin self-check in the past 2 months
Secondary Outcome Measures
- Performance of thorough SSE in the past 1 month [Up to 13 weeks]
Thorough SSE is defined as thoroughly examining each area of the body during the most recent SSE skin self-check in the past 1 month
- Number of SSEs performed (regardless of thoroughness) [Up to 13 weeks]
The total number of self-reported SSEs performed (regardless of their thoroughness)
- Number of body areas examined during SSE [Up to 13 weeks]
The number of body areas (out of 15 total) examined during each SSE will be recorded.
- Benefits to SSE [Up to 13 weeks]
The impact of mySmartCheck on patients' benefits to conducting SSE will be examined using 7 items.
- Barriers to SSE [Up to 13 weeks]
The impact of mySmartCheck on patients' barriers to conducting SSE will be examined using 10 items.
- SSE self-efficacy [Up to 13 weeks]
The impact of MySmartCheck on patient's SSE self-efficacy will be examined using 9 items.
- Level of worry about melanoma [Up to 13 weeks]
The impact of mySmartCheck on patients' level of worry about melanoma will be examined using 2 items.
- Number of health care consultations [Up to 13 weeks]
Survey questions will ask about the number of health care consultations related to skin cancer surveillance in the past 3 months. Questions will include consultation reasons and outcomes.
- Barriers and facilitators to using mySmart check [Up to 13 weeks]
Three multi-item scales will be used to measure barriers and facilitators to using the mySmartCheck program. The first scale is 15 items (5-point response scale from "not at all" to "a lot") adapted from The Internet Impact and Effectiveness Questionnaire. This scale measures patients' perceptions of an Internet intervention in terms of the program's effectiveness in resolving their targeted health condition. The second scale includes 18 items (3-point response scale from "not a problem" to "a major problem") adapted from the Internet Intervention Adherence Questionnaire. This scale is used to identify obstacles and barriers that interfere with using Internet intervention programs. The final scale includes 13 items (4-point response scale from "not at all" to "very") adapted from the Internet Evaluation and Utility Questionnaire. This scale measures patients' experiences and perceptions of an Internet intervention.
Eligibility Criteria
Criteria
Inclusion Criteria:
-
At increased risk for melanoma due to a personal history of treated melanoma without current evidence of disease, a family history of melanoma in a first-degree relative, and/or having a high-risk mole phenotype (i.e., >= 50 normal moles or >= 1 abnormal mole [dysplastic nevus]).
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Access to a computer connected to the Internet.
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Not adherent to SSE recommendations (i.e., did not conduct a thorough SSE during each of the previous 3 months).
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Able to speak and read English.
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Able to provide informed consent.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Rutgers Cancer Institute of New Jersey | New Brunswick | New Jersey | United States | 08903 |
Sponsors and Collaborators
- Rutgers, The State University of New Jersey
- National Cancer Institute (NCI)
Investigators
- Principal Investigator: Sharon Manne, PhD, Rutgers Cancer Institute of New Jersey
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- Pro20170000597
- NCI-2018-02006
- Pro20170000597
- 131707
- P30CA072720