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Efficacy of Wrist Acupressure Band on Sleep Quality in Medical Trainees

Efficacy of Wrist Acupressure Band on Sleep Quality in Medical Trainees: A Single-Blinded Cross-Over Randomized Clinical Trial

Status
Enrolling by invitation
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06978855
Enrollment
50
Registered
2025-05-18
Start date
2025-02-11
Completion date
2025-12-30
Last updated
2025-05-22

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

Conditions

Anxiety, Sleep, SLEEP DISTURBANCES Nec in ICD9CM

Brief summary

Background: Medical trainees frequently experience sleep disturbances, with shift work being a major contributing factor impacting their performance and overall wellbeing. Traditional treatments for sleep disorders often involve medications and hypnotics with potential side effects, highlighting the need for alternative strategies. Acupressure, particularly at the P6 (Neiguan) point, has shown promise in improving sleep and reducing anxiety. Objective: This study aimed to evaluate the efficacy of wristband acupressure applied to the P6 point in improving sleep quality, anxiety levels, and overall well-being among medical trainees. Methods: A single-blinded, cross-over randomized controlled trial was conducted at the American University of Beirut Medical Center (AUBMC), involving 10 medical trainees. Participants were randomized in blocks to either the intervention group, receiving wristband acupressure at the P6 point, or the control group, receiving acupressure at a sham point. Standardized, validated questionnaires were used to assess sleep quality (PSQI), anxiety (GAD-7), and well-being (WHO-5) before and after each intervention period. Ethical approval was obtained from the Institutional Review Board, and participant confidentiality was maintained

Interventions

DEVICEWrist band acupressure application to P6 point

The intervention group received standardized instructions for applying the wristband to the P6 acupressure point on their wrist, with daily application scheduled from 8 pm to 8 am. Those who have night shifts will be asked to apply the wrist band for 12 hours after the end of their shift the intervention was applied for 30 days. At the end of the first phase the participants will be asked to avoid applying the wrist band for 7 days, to allow a washout period before crossing over.

DEVICEWrist band acupressure application to sham point

the control group will receive standardized instructions to apply the wristband to a sham point, with daily application from 8 pm to 8 am. Those who have night shifts will be asked to apply the wrist band for 12 hours after the end of their shift. This will occur for 30 days. At the end of the first phase the participants will be asked to avoid applying the wrist band for 7 days, to allow a washout period before crossing over.

Sponsors

American University of Beirut Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
DEVICE_FEASIBILITY
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

Residents, Fellows and Med-4 students at AUB.

Exclusion criteria

* Being enrolled in another sleep study * Currently on Sleep Medications: Benzodiazepines, antihistamines, muscle relaxants, magnesium supplements, herbal supplements that help with sleep including Chamomile, Ashwaghanda and Melatonin * Daily alcohol consumers

Design outcomes

Primary

MeasureTime frameDescription
Pittsburgh Sleep Quality Index1 monthPittsburgh Sleep Quality Index (PSQI) score, ranging from 0 to 21. Higher scores indicate worse sleep quality.

Secondary

MeasureTime frameDescription
Generalized Anxiety Disorder-71 monthGeneralized Anxiety Disorder-7 (GAD-7): Scores range from 0 to 21, with higher scores indicating greater severity of anxiety symptoms.
World Health Organization Well-Being Index (WHO-5)1 monthWorld Health Organization Well-Being Index (WHO-5): Raw scores range from 0 to 25 and are multiplied by 4 to give a percentage score from 0 to 100. Higher scores indicate better well-being.

Countries

Lebanon

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026