None listed
Conditions
Brief summary
The purpose of the study was to prospectively evaluate the utiilty of the two pateint education interventions to faciliate the medical aesthetic treaments decisions of subjects in the two educatoin groups
Interventions
The loss of bone and soft tissue, the redistribution of fat and decreased dermal elasticicy and thickness contribute to the formation of wrinkles and folds, all commonly characterise the inevitable ageing process.
A single formalised and reproducible consultation procedure, would empower the patient to make an informed treatment decision individualised to their specific needs.
The primary objective of this study is to prospectively evaluate the utility of a computer generated software program,
The loss of bone and soft tissue, the redistribution of fat and decreased dermal elasticicy and thickness contribute to the formation of wrinkles and folds, all commonly characterise the inevitable ageing process. A single formalised and reproducible consultation procedure, would empower the patient to make an informed treatment decision individualised to their specific needs. The primary objective of this study is to prospectively evaluate the utility of a computer generated software program, compared to a standardised patient education intervention over a 9 week period. Both the education programs are administered at the Screening visit and then again at the week 9 visit, with the control arm being given the opportunity to complete the software at the completion of their W9 visits. Both education groups are assessed as to the impact of the subjects decision making on medical aesthetic treatments. The software programme takes approximately 45 minutes for the subject to complete and the control group education intervention is administered in the form of an information sheet and is read by the subect and should take no longer that 20 minutes to read and comprehend.
Sponsors
Allergan Australia Pty Ltd
Eligibility
Sex/Gender
All
Age
25 Years to 54 Years
Healthy volunteers
Yes
Inclusion criteria
Female subjects who are cosmetic/aesthetically oriented Female subjects who are current aesthetic clients at the site for >12 months Female subjects that agree that the enrolling clinic will be principal provider of services during the assessment period. Female subjects who are intending to have medical aesthetic procedures during the study Individuals who are classified as being either a "low" or "moderate" user of aesthetic services within the last 12 months defined as follows:- Low - A single treatemnt cycle of BoNT-A and/or filler and/or lasers and/or IPS in the last 12 months Moderate - 2 or more treatment cycles of BoNT-A and/or filler and/or lasers and/or IPL in the last 12 months
Exclusion criteria
Males Female subjects who have received facial filler, facial botulinum toxin or plastic surgery within 3 months of the study Individuals who have had a reaction to medical aesthetic treatments Females who plan to become pregnant during the study Any medical conditon that the investigator deems that the subject would not be suitable to comply with the study
Outcome results
None listed