The Effect of Facial Exercise on the Appearance of Aging
A Pilot Study of the Efficacy of a Facial Exercise Program
1 other identifier
interventional
27
1 country
1
Brief Summary
This study seeks to evaluate the effects of facial exercises on aging of the face.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Sep 2012
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
September 1, 2012
CompletedFirst Submitted
Initial submission to the registry
September 14, 2012
CompletedFirst Posted
Study publicly available on registry
September 20, 2012
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 1, 2013
CompletedStudy Completion
Last participant's last visit for all outcomes
June 1, 2013
CompletedDecember 6, 2021
December 1, 2021
9 months
September 14, 2012
December 2, 2021
Conditions
Outcome Measures
Primary Outcomes (1)
Improvement of face and neck after facial exercise compared to baseline
up to 20 weeks
Study Arms (1)
Facial Exercise
EXPERIMENTALInterventions
Eligibility Criteria
You may qualify if:
- Aged 40-65 years
- No significant medical illness
- No chronic smokers
- Subject with mild to moderate facial atrophy
- Subjects who provide and interest and who understand the importance of consistently executing the program daily.
- Subjects with the willingness and ability to understand and provide informed consent.
You may not qualify if:
- Under 40 years of age, Over 65 years of age
- Pregnant or lactating
- Subjects who have ever had any invasive cosmetic procedure, including facelifts, neck lifts, laser resurfacing, dermabrasion, or liposuction
- Subjects who have non-invasive or minimally invasive cosmetic procedures, such a non-ablative lasers, medium-depth or deeper chemical peels, injectable neurotoxins or fillers, within the past year.
- Subjects who have used topical or oral retinoids within the past year.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Northwestern University Feinberg School of Medicine, Department of Dermatology
Chicago, Illinois, 60611, United States
Study Officials
- PRINCIPAL INVESTIGATOR
Murad Alam, MD
Northwestern University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- PREVENTION
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor in Dermatology, Otolaryngology- Head and Neck Surgery, and Surgery-Organ Transplantation
Study Record Dates
First Submitted
September 14, 2012
First Posted
September 20, 2012
Study Start
September 1, 2012
Primary Completion
June 1, 2013
Study Completion
June 1, 2013
Last Updated
December 6, 2021
Record last verified: 2021-12