Actively Recruiting

Phase Not Applicable
Age: 18Years - 100Years
All Genders
Healthy Volunteers
NCT05389332

A Mobile Health Intervention Among Hispanics

Led by Rutgers, The State University of New Jersey · Updated on 2025-12-16

114

Participants Needed

1

Research Sites

79 weeks

Total Duration

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AI-Summary

What this Trial Is About

Hypothesis: More than 80% of the participants (n=40) will complete the intervention at three month (intervention completion) and the six month follow-up (retention rate as feasibility). More than 70% of the participants will report high overall study satisfaction (acceptability) with the intervention and study. This pre-pilot will inform intervention and procedural refinements for the pilot. Hypothesis: Participants who receive the intervention (n=57) will report more skin cancer-related preventive behaviors (e.g., mean of summed score of sun protection behaviors such as use of sunscreen, etc.) at three month and six month follow-up compared to those in the control condition (n=57, who will receive general information about physical activity and nutrition).

CONDITIONS

Official Title

A Mobile Health Intervention Among Hispanics

Who Can Participate

Age: 18Years - 100Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Self-report as Hispanics
  • 18 years or older
  • No personal history of skin cancer
  • Report more than one skin cancer risk factor
  • Do not engage in sufficient sun protection behaviors
  • Have not conducted a skin self-examination in the past three months
  • Own a smartphone and are willing to use WhatsApp
Not Eligible

You will not qualify if you...

  • Currently being treated for melanoma or nonmelanoma skin cancer

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Rutgers Cancer Institute of New Jersey

New Brunswick, New Jersey, United States, 08901

Actively Recruiting

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Research Team

Z

Zhaomeng Niu, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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