← Eichor
Study identifier: NCT07410936 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Self-Acupressure and Social Jet Lag in Female Health Sciences Students

Condition: Social Jet Lag · Sleep Disturbance · Sleep Quality  ·  Sponsor: Nigde Omer Halisdemir University

PhaseNA
Planned participants120
Who can joinFemale, 18 Years to 25 Years
Healthy volunteersYes

About this study

This randomized, sham-controlled trial aims to evaluate the effects of self-administered acupressure on social jet lag, sleep patterns, and sleep quality in female health sciences students. Participants will be randomly assigned to either a self-acupressure intervention group or a sham self-acupressure control group. The intervention will be performed daily for 12 weeks. Outcomes will be assessed at baseline and at the end of the intervention period, with the primary outcome being the change in social jet lag. Secondary outcomes include changes in sleep quality, daytime sleepiness, and participant blinding assessment.

This description comes directly from the study's public registry record.

Talk to the study team

Pınar Erdoğan, Assoc. Prof.  ·  +905233646954  ·  drpinarerdogan@gmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

Niğde Ömer Halisdemir University HospitalNiğde, Merkez, Turkey (Türkiye)Recruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT07410936