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Rotation and Movement System, Postpartum Cesarean Sections

K

Kars Harakani State Hospital

Status

Completed

Conditions

Breast Feeding, Exclusive

Treatments

Other: Giving side position with patient turning and movement system

Study type

Interventional

Funder types

Other

Identifiers

NCT05499208
KarsHarakani Lazoglu0001

Details and patient eligibility

About

In the first half hour of a cesarean advertisement, the service-oriented mother will not be mobile and will need support to get fit in bed and start getting started. The patient turning and movement system will provide a lot of convenience to the mother who does not have enough support.

With the remote control system, the mother will be easily turned to the desired side in the bed and it will be ensured that she takes the desired position with less pain and more comfort.

Full description

While studies on the Patient Turning and Movement System have been conducted on long-term bedridden patients, there is no scientific study examining its effects in the obstetric field. For the reasons mentioned above, the aim of this research is; The aim of this study is to investigate the effect of Patient Turning and Movement System on postpartum early postpartum breastfeeding success, pain and postpartum comfort in puerperant women who delivered by cesarean section and to contribute to the literature.

Enrollment

150 patients

Sex

Female

Ages

18 to 35 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Being between the ages of 18-35.
  • Primiparity.
  • Having a transverse cesarean section.
  • At least primary school graduate.
  • No high-risk pregnancy.
  • Absence of any complications in the puerperal and newborn during the delivery and postnatal period

Exclusion criteria

  • Having an open wound on the body and/or an allergic disease diagnosis on the skin.
  • Development of puerperal complications (bleeding, infection, fever).
  • At risk of convulsions; have diseases such as eclampsia, epilepsy.
  • Having a body mass index above 40 (morbidly obese).
  • Having any contraindications for breastfeeding.
  • Having chronic opioid, antidepressant, and psychoactive drug use.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

150 participants in 2 patient groups

Giving side position with patient turning and movement system
Experimental group
Description:
On the day she was admitted to the clinic, the pregnant woman was taken to the room with the turning and movement system, the system was introduced and the personal information form was filled. When she came to the clinic from the operating room, the puerperant was placed on the bed with the turning and motion system (side position) and a follow-up form for LATCH, GKO and Lactogenesis Free symptoms was filled in the first three breastfeedings. Before discharge, LATCH, GCS, and Lactogenesis symptoms follow-up forms were filled in the last three breastfeedings. WHO was filled 1-2 hours before discharge. On the 3rd and 4th days after discharge, the lactogenesis symptoms follow-up form was filled by phone.
Treatment:
Other: Giving side position with patient turning and movement system
Control: Assigned Interventions standard care group
No Intervention group
Description:
routine maintenance of the hospital

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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