Anxiety State Clinical Trial
— ambauricOfficial title:
Interest of Acupressing in the Treatment of Preoperative Anxiety and Comfort of Patients Undergoing Oocyte Retrieval in Outpatient Surgery
The objective of this preliminary study is therefore to assess the feasibility, safety and reduction of perioperative anxiety thanks to acupressing. In addition, patients undergoing oocyte retrieval often present postoperatively with nausea, abdominal pain and discomfort. Acupuncture could also help these patients.
Status | Recruiting |
Enrollment | 82 |
Est. completion date | February 2, 2025 |
Est. primary completion date | February 1, 2025 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Patients over 18 years old - Scheduled to undergo an oocyte retrieval in outpatient surgery - Anxiety score = 3 when they arrived in the outpatient unit - Subject is willing and able to provide informed consent - Covered by a national healthcare insurance Non-Inclusion Criteria: - Ear's pavilion infection - Wrist infection - Previous treatment with auriculotherapy or acupuncture - With a planned intervention that does not allow the delay of 45 min delay (+/- 15 min) between the acupuncture treatment and the STAI assessment - Being deprived of liberty or under guardianship Exclusion criteria - Patient having recourse to any treatment or method of anxiolysis the morning of the procedure, after having given her consent - Patient wishing to withdraw from the study |
Country | Name | City | State |
---|---|---|---|
France | Foch Hospital | Suresnes |
Lead Sponsor | Collaborator |
---|---|
Hopital Foch |
France,
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* Note: There are 14 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Anxiety assessement using State-Trait Anxiety Inventory questionnaire between baseline and 45 minutes after treatment. | Anxiety assessed by the State-Trait Anxiety Inventory questionnaire. It consists of an auto-administered test of 20 items evaluating each item from 0 to 3 on the Likert scale (0= almost never, 1 = sometimes, 2 = often, 3 = almost always).
The primary endpoint is the absolute difference in the state anxiety score measured between the baseline measurement and the measurement 45 minutes after treatment. |
Baseline to 45 minutes after treatment | |
Secondary | Absolute difference measurement between the baseline and the immediate preoperative measurement | Anxiety score measured by numeric scale (0-10). 0 corresponding to no anxiety and 10 more anxiety | between baseline to the immediate preoperative measurement | |
Secondary | Absolute difference measurement between inclusion and when leaving the recovery room | Anxiety score measured by numeric scale (0-10). 0 corresponding to no anxiety and 10 more anxiety | before procedure to time when leaving the recovery room (up to 2 hours) | |
Secondary | Absolute difference measurement between baseline and day 1 | Anxiety score measured by numeric scale (0-10). 0 corresponding to no anxiety and 10 more anxiety | up 24 hours after treatment | |
Secondary | Pain score measured by numeric scale when leaving the recovery room | Pain score measured by numeric scale (0-10). 0 corresponding to no pain and 10 more pain | When leaving the recovery room (up to 2 hours) | |
Secondary | Postoperative nausea and vomiting occurring | Proportion of patients declaring postoperative nausea and vomiting occurring during the stay in the recovery room | In the recovery room (up to 2 hours) | |
Secondary | Postoperative retention of urine | Proportion of patients declaring retention of urine or the need for catheterization for absence or delay in urination occurring during the stay in the recovery room | In the recovery room (up to 2 hours) | |
Secondary | Tolerance of acupressing treatment | The presence or absence of pain and discomfort in the recovery room attributed to the treatment of acupuncture by the patient | In the recovery room (up to 2 hours) | |
Secondary | Satisfaction questionnaire | Proportion of patients answering yes to the question "if you had to do it again, would you choose the same technique?" " when leaving the recovery room | In the recovery room (up to 2 hours) | |
Secondary | Quality of sleep measurement | Quality of sleep measured using the SPIEGEL questionnaire the day after treatment. | up 24 hours after treatment |
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