Ear seeds may boost IVF success by calming anxiety
NCT ID NCT07409792
First seen Jun 27, 2026 · Last updated Aug 14, 2026 · Updated 1 time
Summary
This study tests whether a simple ear acupressure technique, called auricular point sticking therapy, can reduce anxiety and improve sleep in women undergoing IVF. 178 women aged 20-45 with anxiety or insomnia will either receive standard IVF care or standard care plus ear acupressure. Researchers will measure stress hormones, sleep quality, and pregnancy rates to see if the added therapy makes a difference.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- auricular point sticking therapy (ear acupressure with Vaccaria seeds)
- What this could lead to
- If it works, this could offer a simple, drug-free way to ease anxiety and improve sleep for women undergoing IVF, potentially increasing pregnancy success.
- What could go wrong
- This is a small, early-stage trial with no blinding, so results may be influenced by placebo effects. The therapy is complementary and not a substitute for standard IVF care.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 178 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Feb 2026
- Expected to finish
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Mar 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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20 to 45 years
- Sex
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Female participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
1.Diagnostic Criteria for Infertility The diagnosis is established in accordance with \*Obstetrics and Gynecology (10th Edition)\* and the \*Guidelines for Diagnosis and Treatment of Infertility (2019)\*. To be eligible, patients must meet the following criteria: 1. Be a woman of reproductive age, between 20 and 45 years old; 2. Have failed to achieve a clinical pregnancy after ≥12 months of regular, unprotected intercourse (or ≥6 months for women aged ≥35). Furthermore, the indication for IVF-ET must be met by satisfying at least one of the following conditions: 1. Ovulatory factor infertility (e.g., hypothalamic amenorrhea or menstrual disorders, pituitary amenorrhea or menstrual disorders, ovarian amenorrhea or menstrual disorders, other endocrine disorders); 2. Pelvic factor infertility (e.g., congenital anomalies of the reproductive system, cervical factors, uterine disorders, tubal and/or peritoneal factors, endometriosis); 3. Male factor infertility (e.g., azoospermia, oligospermia, asthenospermia, teratospermia, isolated abnormal seminal plasma); 4. Unexplained infertility. 2\. Diagnostic Criteria for Anxiety State Diagnosis is based on the diagnostic criteria for anxiety disorders as outlined in the \*Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5)\* and the \*International Classification of Diseases, Eleventh Revision (ICD-11)\*. Eligible patients must meet the following criteria: 1. Score ≥5 on the self-administered Generalized Anxiety Disorder 7-item (GAD-7) scale; 2. Exhibit significant anxiety symptoms: excessive worry not confined to specific circumstances, or disproportionate worry about various aspects of life; 3. Experience associated symptoms, such as: muscle tension or restlessness; symptoms of autonomic hyperactivity (e.g., frequent gastrointestinal symptoms like nausea or abdominal discomfort, palpitations, sweating, trembling, dry mouth); subjective feelings of tension, restlessness, difficulty concentrating, or irritability; 4. Symptoms persist for at least one month and are present most of the time; 5. The symptoms are not better explained by another mental disorder, are not attributable to the physiological effects of a substance or medication (or its withdrawal), and are not a manifestation of another medical condition; 6. The symptoms cause clinically significant distress or impairment in social, occupational, or other important areas of functioning. 3 Diagnostic Criteria for Insomnia Disorder Diagnosis is based on the diagnostic criteria for insomnia disorder as outlined in the \*Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5) and the International Classification of Diseases, Eleventh Revision (ICD-11) 3. Eligible patients must meet the following criteria: 1. Score ≥8 on the self-administered Pittsburgh Sleep Quality Index (PSQI); 2. Report dissatisfaction with sleep quantity or quality, accompanied by one or more of the following symptoms: ① Difficulty initiating sleep (sleep latency \>30 minutes); ② Difficulty maintaining sleep, characterized by frequent awakenings or difficulty returning to sleep after awakenings (wake after sleep onset \>30 minutes); ③ Early morning awakening (waking \>30 minutes earlier than desired) with inability to return to sleep; 3. The sleep disturbance causes clinically significant distress or impairment in social, occupational, educational, academic, behavioral, or other important areas of functioning; 4. The sleep difficulty occurs at least three nights per week and has been present for at least one month; 5. The insomnia is not better explained by and does not occur exclusively during the course of another sleep-wake disorder, mental disorder, or medical condition, and is not attributable to the physiological effects of a substance. Inclusion Criteria: * (1) Patients who meet the above diagnostic criteria and have undergone IVF-ET; (2) Female patients aged 20-45 years, with a BMI of 18-28 kg/m²; (3)The embryo to be transferred is a high-quality frozen-thawed embryo (either a Day-3 embryo with ≥8 cells, uniform blastomere size, and fragmentation rate \<10%, or a blastocyst with a grade of ≥3BB); (4) Willing to provide written informed consent and comply with luteal support therapy and follow-up. Exclusion Criteria: * (1) Unauthorized use of sedatives or anxiolytics during the treatment period; (2) Adherence to auricular point sticking therapy less than 80% (based on patient diary records); (3) Cancellation of the frozen embryo transfer cycle (e.g., due to endometrial transformation failure or sudden onset of ovarian hyperstimulation syndrome); (4) The participant voluntarily requests to withdraw from the study.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Hangzhou Hospital of Traditional Chinese Medicine
Hangzhou, Zhejiang, 310007, China
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