Evidence map›Paper›PMID 38345836›Full record

ArticleJMIR research protocols2024

A Digital Intervention to Improve Skin Self-Examination Among Survivors of Melanoma: Protocol for a Type-1 Hybrid Effectiveness-Implementation Randomized Trial.

Sharon Manne, Carolyn J Heckman, Sara Frederick, Alexis A Schaefer, Christina R Studts, Olga Khavjou, Amanda Honeycutt, Adam Berger, Hao Liu

Open access · goldAbstract read
In one paragraph

Article in JMIR research protocols, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 42% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 1 country.

Sharon ManneRutgers Cancer Institute of New Jersey, New Brunswick, NJ, United States.ORCID https://orcid.org/0000-0002-9304-7822
Carolyn J HeckmanRutgers Cancer Institute of New Jersey, New Brunswick, NJ, United States.ORCID https://orcid.org/0000-0003-1016-3965
Sara FrederickRutgers Cancer Institute of New Jersey, New Brunswick, NJ, United States.ORCID https://orcid.org/0000-0001-5962-6938
Alexis A SchaeferRutgers Cancer Institute of New Jersey, New Brunswick, NJ, United States.ORCID https://orcid.org/0009-0001-2789-2024
Christina R StudtsUniversity of Colorado Anschutz Medical Campus, Aurora, CO, United States.ORCID https://orcid.org/0000-0002-4856-7255
Olga KhavjouRTI International, Research Triangle Park, NC, United States.ORCID https://orcid.org/0000-0003-0805-0769
Amanda HoneycuttRTI International, Research Triangle Park, NC, United States.ORCID https://orcid.org/0000-0003-0166-1399
Adam BergerRutgers Cancer Institute of New Jersey, New Brunswick, NJ, United States.ORCID https://orcid.org/0000-0003-1192-3276
Hao LiuRutgers Cancer Institute of New Jersey, New Brunswick, NJ, United States.ORCID https://orcid.org/0000-0003-0356-7478
Rutgers, The State University of New Jersey · USRTI International · USUniversity of Colorado Anschutz Medical Campus · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAlthough melanoma survival rates have improved in recent years, survivors remain at risk of recurrence, second primary cancers, and keratinocyte carcinomas. The National Comprehensive Cancer Network recommends skin examinations by a physician every 3 to 12 months. Regular thorough skin self-examinations (SSEs) are recommended for survivors of melanoma to promote the detection of earlier-stage, thinner melanomas, which are associated with improved survival and lower treatment costs. Despite their importance, less than a quarter of survivors of melanoma engage in SSEs.

objectivePreviously, our team developed and evaluated a web-based, fully automated intervention called mySmartSkin (MSS) that successfully improved SSE among survivors of melanoma. Enhancements were proposed to improve engagement with and outcomes of MSS. The purpose of this paper is to describe the rationale and methodology for a type-1 hybrid effectiveness-implementation randomized trial evaluating the enhanced MSS versus control and exploring implementation outcomes and contextual factors.

methodsThis study will recruit from state cancer registries and social media 300 individuals diagnosed with cutaneous malignant melanoma between 3 months and 5 years after surgery who are currently cancer free. Participants will be randomly assigned to either enhanced MSS or a noninteractive educational web page. Surveys will be collected from both arms at baseline and at 3, 6, 12, and 18 months to assess measures of intervention engagement, barriers, self-efficacy, habit, and SSE. The primary outcome is thorough SSE. The secondary outcomes are the diagnosis of new or recurrent melanomas and sun protection practices.

resultsMultilevel modeling will be used to examine whether there are significant differences in survivor outcomes between MSS and the noninteractive web page over time. Mixed methods will evaluate reach, adoption, implementation (including costs), and potential for maintenance of MSS, as well as contextual factors relevant to those outcomes and future scale-up.

conclusionsThis trial has the potential to improve outcomes in survivors of melanoma. If MSS is effective, the results could guide its implementation in oncology care and nonprofit organizations focused on skin cancers. INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID): RR1-10.2196/52689.

Indexed as

cancer survivorshipdigital interventionsmelanomaskin self-examinations

Identifiers

PMID38345836
PMCPMC10897801
OpenAlexW4391754362

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.