Effect of Foot Massage on Postpartum Comfort and Pain Level of the Mothers Who Had Vaginal Birth
Postpartum Disorder, Massage
About this trial
This is an interventional supportive care trial for Postpartum Disorder focused on measuring analgesia, massage, midwifery, pain, postpartum period
Eligibility Criteria
Inclusion Criteria:
- primipara mothers (who had their first birth),
- mothers who had normal vaginal delivery,
- those who had undergone episiotomy,
- who were volunteered to participate in the study,
- who were on the first day of delivery (first 24 hours),
- who had no complications in the infant and the baby,
- age of whom ranged from 18 to 35,
- those who did not apply or receive any other complementary therapy,
- mothers who did not have any wound, infection or discomfort etc. on their feet,
- mothers who can read and write
Exclusion Criteria:
- mothers with any systemic disease
- mothers who dislike foot massage during practice
- early discharge mothers
- mothers who applied another massage technique
- mothers who take the analgesic drug unnecessarily
Sites / Locations
- Ege University
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
Study Group
Control Group
The first session of the foot massage was performed after mothers were taken to the postpartum service and after the effect of the first analgesia had elapsed (4-6 hours after birth). The researcher prepared the mother for foot massage (foot care, proper position, etc.) and gave a total of 20-minute massage of foot massage, 10 minutes for each foot. VAS was repeated immediately after the first session (in the 20th minute) and after 30 minutes (in the 50th minute). The second session was performed on the second day, 20-24 hours after the first session (before the discharge). The VAS was analyzed before the second (last) session (0th minute), and the VAS was repeated immediately after the application (20th minute) and 30 minutes (50th minute), and the PCS was administered for the last time. Administered analgesics were recorded in the DFC and the administration made with package leaflet was supported.
Routine procedures were applied and VAS was repeated at the same time periodical as the study group mothers (0th, 20th and 50th minute) and after 20-24 hours (before discharge), at the same time intervals (0th, 20th and 50th minute) pain status was measured by using VAS and PCS was administered for the last time and analgesics administered were recorded on the DFC.