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The Effect of Reflexology on Pain, Comfort and Breastfeeding Self-Efficacy

Y

Yuzuncu Yıl University

Status

Completed

Conditions

Reflexology

Treatments

Behavioral: Reflexology

Study type

Interventional

Funder types

Other

Identifiers

NCT06769958
Reflexology

Details and patient eligibility

About

This study was conducted to determine the effects of reflexology applied to mothers with headache due to spinal anesthesia after Cesarean delivery on pain, comfort and breastfeeding self-efficacy levels. The study, which was conducted with a single-blind, randomized controlled experimental design, was conducted between April 2024 and August 2024 at the Department of Obstetrics and Pediatrics, SBU Van Training and Research Hospital with mothers who had cesarean delivery under spinal anesthesia and had postpartum headache (Intervention group=30, Control group=30). Foot reflexology was applied to the mothers in the intervention group for a total of 30 minutes, 15 minutes on each foot. The control group was not subjected to any intervention other than routine nursing practices. Personal Information Form, Visual Analog Scale (VAS), Postpartum Comfort Scale (PPSC) and Breastfeeding Self-Efficacy Scale (BSSE) were used as data collection tools.

Enrollment

60 patients

Sex

Female

Ages

18 to 45 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 18 years and older,
  • performing SD under spinal anesthesia,
  • experiencing postpartum headaches,
  • Caesarean section performed at 37-42 weeks of gestation,
  • giving only one live birth,
  • open to written or oral communication,
  • at least a primary school graduate,
  • no complications during pregnancy,
  • mothers who agreed to participate in the study

Exclusion criteria

  • Performing a cesarean section at periods other than 37-42 weeks of gestation,
  • caesarean section under general anesthesia,
  • have health problems such as fractures, dislocations, phlebitis, arthritis, burns, wounds, eczema, fungus or inflammation in the foot tissue,
  • with disease of the cardiovascular system,
  • with chronic diseases such as hypertension or diabetes mellitus,
  • Postpartum controlled analgesia administered,
  • mothers with psychiatric diagnoses such as anxiety and depression

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Single Blind

60 participants in 2 patient groups

Reflexology
Experimental group
Treatment:
Behavioral: Reflexology
Control
No Intervention group

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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