A Motivational Enhancement Approach to Skin Cancer Prevention

This study has been completed.
Sponsor:
Information provided by:
Oregon Health and Science University
ClinicalTrials.gov Identifier:
NCT00705887
First received: June 25, 2008
Last updated: NA
Last verified: June 2008
History: No changes posted
  Purpose

The specific aims of this research are:

Aim 1 - To describe the UV protection behaviors and beliefs of young adult patients in a dermatology clinic.

Aim 2 - To examine whether or not the UV protection behaviors and beliefs of young adult dermatology patients are associated with age, gender, level of education, marital status, contact with skin cancer, time outdoors, skin type, the reason for their visit, and the date of data collection.

Aim 3 - To test the efficacy of a motivational enhancement approach to UV protection counseling for young adult dermatology patients, as manifested by favorable changes in UV protection stages of change, UV protection self-efficacy, and UV protection attitudes.


Condition Intervention
Ultraviolet Rays
Motivation
Behavioral: Brief Motivational Enhancement Intervention

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Single Blind (Subject)
Primary Purpose: Prevention
Official Title: The Feasibility of a Motivational Enhancement Approach to Skin Cancer Prevention in a Sample of Young Adult Patients

Resource links provided by NLM:


Further study details as provided by Oregon Health and Science University:

Primary Outcome Measures:
  • UV Protection Stages of Change [ Time Frame: 6 months ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • UV Protection Attitudes [ Time Frame: 6 months ] [ Designated as safety issue: No ]
  • UV Protection Self-Efficacy [ Time Frame: 6 months ] [ Designated as safety issue: No ]

Enrollment: 82
Study Start Date: September 2006
Study Completion Date: June 2007
Primary Completion Date: June 2007 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
No Intervention: Control
Brochure from the American Academy of Dermatology on protecting your skin from UV rays.
Experimental: Intervention
Participation in a brief motivational enhancement session. These participants also received the same American Academy of Dermatology brochure on protecting your skin from UV rays.
Behavioral: Brief Motivational Enhancement Intervention
The motivational enhancement intervention lasted 5-8 minutes and consisted of gaining the client's permission to address the topic of skin cancer prevention, exchanging information through the elicit-provide-elicit strategy of information exchange, and summarization/ conclusion based on verbal and nonverbal cues from the participant.
Other Name: Adaptation of Motivational Interviewing

Detailed Description:

Although skin cancer is the most common form of cancer in the United States, it is highly preventable by reducing exposure to ultraviolet (UV) radiation. However, recent primary prevention efforts have been inadequate in evoking behavior change, as manifested by increasing rates of ultraviolet radiation exposure, particularly among young adults. These findings indicate the need to research novel approaches to skin cancer prevention.

Motivational enhancement techniques facilitate patient-centered, directive discussions wherein practitioners provide clear structure and encourage patients to play an active role in the consultation. The use of motivational enhancement techniques for health behavior change in medical settings has thus far yielded encouraging results for other health behavior change topics, but research has not yet investigated the application of these techniques to skin cancer prevention discussions.

  Eligibility

Ages Eligible for Study:   18 Years to 30 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Dermatology patient presenting for scheduled appointment
  • 18-30 years old

Exclusion Criteria:

  • Seeking treatment for sunburn
  • Unable to read and understand English
  • Having previously received medical treatment from the interventionist
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00705887

Locations
United States, Utah
Central Utah Clinic, Dermatology
Provo, Utah, United States, 84604
Sponsors and Collaborators
Oregon Health and Science University
Investigators
Principal Investigator: Christina P Linton, FNP-BC, PhD Oregon Health and Science University
Study Chair: Nancy Press, PhD Oregon Health and Science University
  More Information

No publications provided

Responsible Party: Christina P. Linton, FNP-BC, PhD, Oregon Health & Science University
ClinicalTrials.gov Identifier: NCT00705887     History of Changes
Other Study ID Numbers: IRB00002996
Study First Received: June 25, 2008
Last Updated: June 25, 2008
Health Authority: United States: Institutional Review Board

Keywords provided by Oregon Health and Science University:
Ultraviolet Rays
Motivation
Health Education
Randomized Controlled Trial
Health Knowledge, Attitudes, Practice

ClinicalTrials.gov processed this record on October 19, 2014