Acupressure Applied After Cesarean Section on Postpartum Pain

NCT ID: NCT06138288

Last Updated: 2024-01-09

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

60 participants

Study Classification

OBSERVATIONAL

Study Start Date

2023-11-20

Study Completion Date

2023-12-30

Brief Summary

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Pressure applied according to the principles of acupressure limits the pain limit, reduces the secretion of endorphins, which is a neurochemical, reduces the tension in the muscles, reduces the amount of oxygen in the blood flow, and finally provides duration and relaxation. Acupressure application is becoming more and more common nowadays because it is a noninvasive, safe, easy-to-apply and effective method without side effects. It seems that there is a limit to the study in which group acupressure applications in the literature are examined together on pain and comfort after cesarean section. In these basic points, the expectations of achieving postpartum pain and postpartum comfort of acupressure applied after cesarean delivery in this study. The circle of the research; There will be women who will have repeated cesarean section in a private Obstetrics Clinic in Famagusta. Women will be separated from two groups, one group will continue acupressure and the other group will do routine care. Visual analog scale and end-of-birth comfort procedure will be applied to women before and after the application.

Detailed Description

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Pressure applied according to the principles of acupressure limits the pain limit, reduces the secretion of endorphins, which is a neurochemical, reduces the tension in the muscles, reduces the amount of oxygen in the blood flow, and finally provides duration and relaxation. Acupressure application is becoming more and more common nowadays because it is a noninvasive, safe, easy-to-apply and effective method without side effects. It seems that there is a limit to the study in which group acupressure applications in the literature are examined together on pain and comfort after cesarean section. In these basic points, the expectations of achieving postpartum pain and postpartum comfort of acupressure applied after cesarean delivery in this study. The circle of the research; There will be women who will have repeated cesarean section in a private Obstetrics Clinic in Famagusta. Women will be separated from two groups, one group will continue acupressure and the other group will do routine care. Visual analog scale and end-of-birth comfort procedure will be applied to women before and after the application.

Conditions

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Postpartum Disorder Cesarean Section Complications

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

OTHER

Study Groups

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acupressure group

Women who are in acupressure will apply the application after cesarean section 2nd hour after applying the data collection forms (descriptive features formula, VAS, WHO). For women on acupressure, the application will be applied manually to the SP6, P6 and L14 points in the order indicated by the drawing with the index or middle finger, 1-1.5 cm depth for 5 seconds, pressing for 5 seconds, resting for 2 seconds and continuing for 2 minutes to go. will be with you. VAS will be filled again after the application.

acupressure

Intervention Type BEHAVIORAL

The acupressure points to be used in the research are located on the inner side of the lower leg, 4 fingers above the ankle and on the spleen meridian behind the tibia (SP6), which was previously effective in reducing pain, and located three fingers above the wrist (in the middle of the 2nd metacarpal bone, on the dorsum of the hand, adjacent The points determined as P6 (located between the metacarpal bones) and LI4 located in the space between the thumb and index finger (between the 1st and 2nd metacarpal bones of the hand, in the middle of the 2nd metacarpal bone on the radial side) were applied by a certified researcher to women in the acupressure group. will be done

control group

No interventions assigned to this group

Interventions

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acupressure

The acupressure points to be used in the research are located on the inner side of the lower leg, 4 fingers above the ankle and on the spleen meridian behind the tibia (SP6), which was previously effective in reducing pain, and located three fingers above the wrist (in the middle of the 2nd metacarpal bone, on the dorsum of the hand, adjacent The points determined as P6 (located between the metacarpal bones) and LI4 located in the space between the thumb and index finger (between the 1st and 2nd metacarpal bones of the hand, in the middle of the 2nd metacarpal bone on the radial side) were applied by a certified researcher to women in the acupressure group. will be done

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* agreeing to participate in the research,
* be between the ages of 18-49,
* To give birth by cesarean section between 37-40 weeks,
* Having a healthy and live birth at the end of a single pregnancy,
* Receiving spinal anesthesia
* Being able to read and write Turkish and be open to communication.

Exclusion Criteria

* Absence of pain in the 2nd hour postpartum
* Having a cesarean delivery after a risky pregnancy,
* Having a chronic illness
* Having severe systemic disease
* Not receiving spinal anesthesia
* Having a body mass index over 25,
* Have previous acupressure experience.
Minimum Eligible Age

18 Years

Maximum Eligible Age

49 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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Eastern Mediterranean University

OTHER

Sponsor Role lead

Responsible Party

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Hilal Begüm Çayır

Nurse

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Hilal Begum Cayır

Famagusta, , Cyprus

Site Status

Countries

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Cyprus

References

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Cayir HB, Abic A. The effect of acupressure on postpartum pain and comfort after cesarean delivery: a randomized controlled trial. Women Health. 2024 Nov-Dec;64(10):892-903. doi: 10.1080/03630242.2024.2428793. Epub 2024 Nov 12.

Reference Type DERIVED
PMID: 39532534 (View on PubMed)

Other Identifiers

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ETK00-2023-0107

Identifier Type: -

Identifier Source: org_study_id

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