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The Effect of Facial Exercise on the Appearance of Aging

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ClinicalTrials.gov Identifier: NCT01689012
Recruitment Status : Completed
First Posted : September 20, 2012
Last Update Posted : March 3, 2015
Sponsor:
Information provided by (Responsible Party):
Murad Alam, Northwestern University

Brief Summary:
This study seeks to evaluate the effects of facial exercises on aging of the face.

Condition or disease Intervention/treatment Phase
Aging Behavioral: Facial Exercise Not Applicable

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 27 participants
Intervention Model: Single Group Assignment
Masking: Single (Outcomes Assessor)
Primary Purpose: Prevention
Official Title: A Pilot Study of the Efficacy of a Facial Exercise Program
Study Start Date : September 2012
Actual Primary Completion Date : June 2013
Actual Study Completion Date : June 2013

Resource links provided by the National Library of Medicine


Arm Intervention/treatment
Experimental: Facial Exercise Behavioral: Facial Exercise



Primary Outcome Measures :
  1. Improvement of face and neck after facial exercise compared to baseline [ Time Frame: up to 20 weeks ]


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Ages Eligible for Study:   40 Years to 65 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • 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.

Exclusion Criteria:

  • 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.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01689012


Locations
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United States, Illinois
Northwestern University Feinberg School of Medicine, Department of Dermatology
Chicago, Illinois, United States, 60611
Sponsors and Collaborators
Northwestern University
Investigators
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Principal Investigator: Murad Alam, MD Northwestern University

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Responsible Party: Murad Alam, Professor in Dermatology, Otolaryngology- Head and Neck Surgery, and Surgery-Organ Transplantation, Northwestern University
ClinicalTrials.gov Identifier: NCT01689012     History of Changes
Other Study ID Numbers: STU68255
First Posted: September 20, 2012    Key Record Dates
Last Update Posted: March 3, 2015
Last Verified: March 2015