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Effects of auricular gua sha combined with auricular acupressure on sleep quality in young and middle-aged patients with insomnia

Effects of auricular gua sha combined with auricular acupressure on sleep quality in young and middle-aged patients with insomnia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN67031646
Enrollment
90
Registered
2026-03-27
Start date
2023-03-17
Completion date
Unknown
Last updated
2026-04-14

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

Conditions

Insomnia Mental and Behavioural Disorders

Interventions

Group A (control group): Auricular acupressure once weekly for 4 weeks. Cowherb seeds affixed to auricular acupoints (Shenmen, Endocrine, Heart, Subcortical, with pattern-based additions). Participant

Sponsors

School of Nursing, Medical College of Soochow University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1. In accordance with the diagnostic criteria of insomnia in the Chinese Guidelines for the Diagnosis and Treatment of Insomnia in Adults (2017 edition) 2. ISI score >=8 points 3. Age >=18 years old, regardless of gender

Exclusion criteria

Exclusion criteria: 1. Those suffering from major organic diseases or mental and psychological diseases 2. Those who have recently planned to have a baby or are breastfeeding or pregnant 3. Ear skin with inflammation, eczema, ulcers, frostbite or larger scar organizers 4. People who are allergic to the tape or have other serious adverse events and are unable to complete the trial

Design outcomes

Secondary

MeasureTime frame
1. Sleep quality measured using Pittsburgh Sleep Quality Index (PSQI) at three time points: baseline (T0), after the fourth intervention (T4), and 1 month post-intervention (T5) 2. Anxiety measured using Hospital Anxiety and Depression Scale – Anxiety subscale (HADS-A) at six time points: baseline (T0), weekly during the 4-week intervention period (T1, T2, T3, T4), and 1 month post-intervention (T5) 3. Depression measured using Hospital Anxiety and Depression Scale – Depression subscale (HADS-D) at six time points: baseline (T0), weekly during the 4-week intervention period (T1, T2, T3, T4), and 1 month post-intervention (T5)

Countries

China

Contacts

Public ContactLi Tian
tianlisz@suda.edu.cn+86 138 6259 6317

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Apr 17, 2026