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Facial Exercise and Daily Habit Modification Program for Skin Quality and Wrinkle Severity in Middle-Aged Women

Effects of a Combined Antioxidant Nutrition and Facial Exercise Program on Skin Quality and Wrinkle Severity in Middle-Aged Women

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07792460
Enrollment
204
Registered
2026-08-28
Start date
2026-09-01
Completion date
2026-11-24
Last updated
2026-08-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Facail Skin Aging

Brief summary

This randomized controlled trial will evaluate the effectiveness of a 12-week program combining facial muscle exercises and daily habit modification for improving skin quality and reducing wrinkle severity in middle-aged women. Participants will be randomly allocated to an intervention group receiving the structured program or to a control group maintaining their usual routine. Skin-related outcomes will be assessed at baseline and after 12 weeks using standardized objective measurements.

Interventions

BEHAVIORALFacial Exercise and Daily Habit Modification Program

A 12-week structured program consisting of facial muscle exercises combined with daily habit modification related to skin health

Sponsors

University of Zakho
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
45 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

nclusion Criteria: Female participants aged 45-50 years. Willing and able to participate in the 12-week intervention program. Willing to maintain their usual skincare routine and comply with the study procedures. Able to provide informed consent.

Exclusion criteria

Current smoking. Facial aesthetic procedures such as botulinum toxin injections, dermal fillers, laser treatment, chemical peels, or similar procedures within the predefined period before enrollment. Current dermatological disease or skin condition that may affect facial skin measurements. Uncontrolled chronic medical conditions that may influence skin health or participation in the intervention. Planned initiation of new skincare treatments, cosmetic products, or aesthetic procedures during the 12-week study period. Inability to perform the facial exercise program safely or comply with the study procedures

Design outcomes

Primary

MeasureTime frameDescription
Change in Wrinkle-Severity Reduction IndexBaseline to 12 weeksChange in the mean bilateral crow's feet wrinkle depth (mm) from baseline to week 12, measured using Antera 3D. Three measurements will be obtained from each side, and the mean of the six measurements will be used as the participant-level value. Lower values indicate reduced wrinkle depth

Countries

Iraq

Contacts

CONTACTdalshad m abdulrehman, ph.D .
dlshadm079@gmail.com009647501891419

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 29, 2026