NCT07792460

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.

Trial Health

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Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
204

participants targeted

Target at P75+ for not_applicable

Timeline
3mo left

Started Sep 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
not yet recruiting

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

First Submitted

Initial submission to the registry

August 25, 2026

Completed
3 days until next milestone

First Posted

Study publicly available on registry

August 28, 2026

Completed
4 days until next milestone

Study Start

First participant enrolled

September 1, 2026

Expected
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 24, 2026

Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

November 24, 2026

Last Updated

August 28, 2026

Status Verified

August 1, 2026

Enrollment Period

3 months

First QC Date

August 25, 2026

Last Update Submit

August 25, 2026

Conditions

Outcome Measures

Primary Outcomes (1)

  • Change in Wrinkle-Severity Reduction Index

    Change 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

    Baseline to 12 weeks

Study Arms (2)

intervention group

EXPERIMENTAL

Participants in the intervention group will complete a 12-week structured facial exercise program combined with daily habit modification related to skin health

Behavioral: Facial Exercise and Daily Habit Modification Program

control group

NO INTERVENTION

Participants in the control group will maintain their usual daily routine and will not receive the structured facial exercise or daily habit modification program during the 12-week study period

Interventions

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

intervention group

Eligibility Criteria

Age45 Years - 50 Years
Sexfemale
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Fitness Centers and Gyms in Duhok

Duhok, Duhok Governorate, 42001, Iraq

Location

Central Study Contacts

dalshad m abdulrehman, ph.D .

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
principal investigator

Study Record Dates

First Submitted

August 25, 2026

First Posted

August 28, 2026

Study Start (Estimated)

September 1, 2026

Primary Completion (Estimated)

November 24, 2026

Study Completion (Estimated)

November 24, 2026

Last Updated

August 28, 2026

Record last verified: 2026-08

Data Sharing

IPD Sharing
Will not share

Individual participant data are not planned to be shared. Only aggregated, de-identified study results will be reported

Locations