Positive Exposure: A Photography and Video Intervention for Individuals With Craniofacial Differences
NCT ID: NCT00340964
Last Updated: 2019-12-12
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
44 participants
OBSERVATIONAL
2005-06-13
2014-01-06
Brief Summary
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Patients ages 12 years and older who have craniofacial conditions may be eligible for this pilot study. About 30 people will participate. Participants will be asked to provide the diagnosis of their craniofacial conditions. They will also be asked how many surgeries and what kinds they have had over the years, and how old they were at the time of the surgeries. This information will not be connected to participants' names and will be stored in a database protected by password.
There are three parts to the study. In Part 1, patients will be asked to write a personal reflection (for as long as they wish) on their experiences of having their picture taken and being video taped. They will also fill out a brief survey, taking about 15 minutes. They are able to do this at home and will mail their responses to the researchers. In Part 2, they will take part in a photo-shoot (about 1 hour) conducted by the founder and program director of Positive Exposure and then take part in a video interview (about 30 minutes) conducted by a co-investigator from that organization. In Part 3, to take place 1 month following the photo-shoot, participants will write a final reflection that describes their experiences with Positive Exposure and then fill out another brief survey (about 10 minutes). Surveys used in the study will be the Self-Esteem Scale, Perceived Social Stigma Scale, and State Hope Scale. Photo-shoots and video interviews will be held at the studio of Positive Exposure in New York City or, if necessary, at a location closer to the participant's home. The projected time line of this pilot study is 10 months.
Direct benefits are not the goal of participation in this study. However, participants may enjoy the photo-shoots and video interviews, as well as the process of reflecting and sharing their life and photo experiences with others. This pilot study will be a starting point for future research into Positive Exposure for adolescents and adults with visible genetic conditions.
Detailed Description
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Conditions
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Keywords
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Eligibility Criteria
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Inclusion Criteria
* Participants must have a clinically diagnosed craniofacial condition.
* Participants must be able to speak and write in English. However, if individuals have trouble writing (i.e. dyslexia or dysgraphia), they can tape record their personal reflections, which will be transcribed verbatim for analysis.
Exclusion Criteria
* If the individual does not speak English.
* If the individual has been photographed by Rick Guidotti or another professional photographer in the past.
* If the individual has been video-interviewed by Diane McLean.
* If the individual has cognitive impairments that would preclude successfully completing the various steps of the study.
12 Years
20 Years
ALL
No
Sponsors
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National Human Genome Research Institute (NHGRI)
NIH
Principal Investigators
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Barbara B Biesecker
Role: PRINCIPAL_INVESTIGATOR
National Human Genome Research Institute (NHGRI)
Locations
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National Human Genome Research Institute (NHGRI), 9000 Rockville Pike
Bethesda, Maryland, United States
Countries
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References
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Dollinger SJ. Physical attractiveness, social connectedness, and individuality: an autophotographic study. J Soc Psychol. 2002 Feb;142(1):25-32. doi: 10.1080/00224540209603882.
Eiserman W. Unique outcomes and positive contributions associated with facial difference: expanding research and practice. Cleft Palate Craniofac J. 2001 May;38(3):236-44. doi: 10.1597/1545-1569_2001_038_0236_uoapca_2.0.co_2.
Jones B. 'Drop 'em Blossom'--clinical photography and patient dignity. J Audiov Media Med. 1996 Jun;19(2):85-6. doi: 10.3109/17453059609023011. No abstract available.
Other Identifiers
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05-HG-N173
Identifier Type: -
Identifier Source: secondary_id
999905173
Identifier Type: -
Identifier Source: org_study_id