Reflexology Hand Massage After Cesarean Section

Condition(s) studied

Investigational drug(s) / intervention(s)

Reflexology Hand Massage: A 20-minute reflexology hand massage administered by the researcher at the 4th postoperative hour following an elective cesarean delivery. This intervention involves applying targeted manual pressure to specific reflexology points on both hands to promote relaxation, reduce postoperative state anxiety, and support hemodynamic stability.

Stroking Hand Massage: A 20-minute simple stroking hand massage administered by the researcher at the 4th postoperative hour following an elective cesarean delivery. This placebo intervention involves gentle, superficial strokes on the hands without exerting any pressure on specific reflex points. It is designed solely to control for the time and physical attention provided to the experimental group.

Study summary

Background: Globally, cesarean section (CS) rates are rapidly increasing. Although cesarean delivery is a life-saving surgical intervention, it can lead to adverse outcomes such as anxiety, decreased maternal satisfaction, and alterations in hemodynamic parameters. Hand massage, as a complementary nursing intervention, is considered an effective method for alleviating these issues by promoting physiological and psychological well-being.

Objective: The aim of this study is to examine the effects of reflexology hand massage and stroking hand massage on anxiety, satisfaction, and hemodynamic parameters in women during the early postoperative period following a cesarean section.

Methods: This study is designed as a single-blind, randomized, placebo-controlled trial. The study population will consist of women who undergo cesarean delivery and are hospitalized in the Obstetrics and Gynecology Ward of Dokuz Eylul University Research and Application Hospital. The study sample will include women aged 20-35 years who undergo a term, elective cesarean delivery between April 2026 and January 2027, and are at their 4th postoperative hour. The experimental group will receive a 20-minute reflexology hand massage, while the control group will receive a 20-minute stroking hand massage (placebo). Due to the single-blind nature of the study, participants will only be informed that they will receive a "hand massage," without specifying the exact technique (reflexology or stroking). Satisfaction will be measured using a Visual Analog Scale (VAS), and anxiety will be measured using the State Anxiety Inventory (STAI) before the intervention and 30 minutes after the massage application. Data obtained from the study will be analyzed using the SPSS (IBM SPSS Statistics, Version 25) software. Descriptive statistics will be presented as mean, standard deviation, and median (minimum-maximum) for continuous variables, and as frequencies and percentages for categorical variables. The conformity of the data to normal distribution will be evaluated using the Kolmogorov-Smirnov and Shapiro-Wilk tests. For the comparison of continuous variables between groups, the Independent Samples t-test will be used for normally distributed data, and the Mann-Whitney U test for non-normally distributed data. For within-group comparisons of time-dependent measurements, Repeated Measures ANOVA will be applied if the normality assumption is met, whereas the Friedman test will be used if it is not met. To compare time-dependent changes between groups, a two-way repeated measures ANOVA will be utilized for normally distributed data, and Generalized Linear Models or appropriate non-parametric methods will be employed for non-normally distributed data. Categorical variables will be compared using the Chi-square test or Fisher's Exact test when necessary. The statistical significance level will be set at p \< 0.05 for all analyses.

Eligibility

Primary outcome measure(s)

• Change in State Anxiety Levels — Baseline (before the intervention at the 4th postoperative hour) and 30 minutes after the completion of the 20-minute massage.
  Anxiety will be assessed using the State Anxiety Inventory (STAI). The state subscale consists of 20 items rated on a 4-point Likert scale. Total scores range from 20 to 80. Higher scores indicate higher levels of state anxiety.

Trial sites (1)

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