Self-acupressure to improve social jet lag in female health sciences students
Official title: Effects of Self-Acupressure on Social Jet Lag, Sleep Patterns, and Sleep Quality in Female Health Sciences Students: A Sham-Controlled Randomized Trial
Run by Nigde Omer Halisdemir University · NCT07410936 · Data updated 2026-11-12
This randomized trial tests whether daily self-acupressure can improve social jet lag and sleep quality in 18-25 year-old female health sciences students compared with a sham procedure.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years to 25 Years |
| Sex | Women only |
| Enrollment | 120 (estimated) |
| Sponsor | Nigde Omer Halisdemir University Academic / other |
| Locations | 1 site (Niğde, Merkez) |
| Status | Recruiting |
| Started | April 24, 2026 |
| Main results expected | December 15, 2026 |
| Study ends | December 15, 2026 |
| Registry record updated | August 24, 2026 |
| Trial ID | NCT07410936 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are 18-25 year-old female undergraduate students in midwifery or medical programs with regular schedules who can commit to daily 12-week practice and complete sleep diaries.
✕Probably not a fit
Individuals with diagnosed sleep disorders, those on medications affecting sleep, shift or night workers, or those planning travel across time zones during the study may not benefit or participate.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This is a randomized, parallel-group, sham-controlled trial conducted over 12 weeks among female health sciences students. Participants are assigned to either a self-acupressure intervention at specific points (HT7, SP6, Yintang) or a sham procedure at non-therapeutic points. Both groups complete daily practice and sleep questionnaires, with baseline and end-of-study assessments focusing on social jet lag as the primary outcome and sleep quality and daytime sleepiness as secondary outcomes. The study aims to determine if self-administered acupressure can reduce circadian disruption related to social schedules without pharmacological therapy. Training is standardized, and a blinding assessment is included to gauge participant perceptions of group assignment.
Why it matters
Potential benefit: If successful, participants may experience reduced social jet lag and better sleep quality, with a simple, self-administered non-drug approach.
How similar studies have gone: Previous trials of non-pharmacological self-administered sleep interventions have shown mixed but promising improvements in sleep parameters in young adults.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Female undergraduate students enrolled in midwifery or medical programs * Age 18 to 25 years * Regular academic schedule (work/school days and free days identifiable) * Willingness to participate and provide written informed consent * Ability to comply with daily self-acupressure practice for 12 weeks * Ability to complete sleep questionnaires and sleep diary Exclusion Criteria: * Current diagnosis of a sleep disorder requiring medical treatment (e.g., obstructive sleep apnea, narcolepsy) * Use of medications known to significantly affect sleep or circadian rhythms (e.g., hypnotics, stimulants) * Shift work or night work during the study period * Transmeridian travel (≥2 time zones) within the past 4 weeks or planned during the study period * Chronic medical or psychiatric condition that may significantly affect sleep * Current pregnancy
Where it's running
-
Niğde Ömer Halisdemir University Hospital
Niğde, Merkez, Turkey (Türkiye) Recruiting
Study contacts
- Study coordinator: Pınar Erdoğan, Assoc. Prof.
- Email: drpinarerdogan@gmail.com
- Phone: +905233646954
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Improving Sleep for Older Adults in the Emergency Department
This project tests whether wearing a Fitbit overnight can help understand and improve sleep for adults 70 and older in the emergency department who are likely to be admitted.
-
Physical activity habits and sleep/ breathing in obstructive sleep apnea
This study tests whether daily physical activity habits affect sleep quality and breathing measurements in people with obstructive sleep apnea who are on CPAP therapy.
-
Shoulder pain patients: see if breathing and chest exercises help pain and sleep
This study tests whether adding respiratory muscle strengthening and diaphragmatic breathing to shoulder rehab can reduce pain and improve sleep in adults with chronic shoulder pain.
-
Virtual Reality-Based Hypnotherapy to Help Pain, Sleep, and Mood in Spinal Cord Injury
Adults with spinal cord injury will try adding short VR-based hypnotherapy sessions to their standard physiotherapy to see if it reduces pain and improves sleep and mood.
-
Telephone-Coached Sleep Bibliotherapy for Dementia Caregivers
This study tests whether an 8-week, telephone-guided sleep self-help program helps informal caregivers of people with dementia sleep better.
-
Sleep detection in long-term care residents
This study tests how well contactless sleep sensors track sleep patterns in older adults living in long-term care facilities.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.