ClinicalTrials.gg
RecruitingNCT07880587Updated Oct 19, 2026

Reflexology Hand Massage After Cesarean Section

An interventional study of Reflexology Hand Massage and Stroking Hand Massage in Cesarean Section, Anxiety and Postoperative Period, sponsored by Dokuz Eylul University. Recruiting at 1 site in Turkey (Türkiye). Open to female participants aged 20 Years to 35 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-10-19.

Sponsored by Dokuz Eylul University · Not applicable, Interventional, and Supportive care

From the registry’s dates

  • Started Jun 2026; still recruiting 3 months later.
Updated Oct 19, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
40
Allocation
Randomized
Ages
20 Years to 35 Years
Sex
Female
01

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.

Read the detailed description

Cesarean section (CS) rates are rapidly increasing worldwide. Although cesarean delivery is a life-saving surgical procedure, the anxiety it causes can lead to negative consequences such as decreased maternal satisfaction and changes in hemodynamic parameters. Manual massage, which is among the complementary nursing interventions, is considered an effective method in reducing these problems by supporting physiological and psychological well-being.

02

Conditions studied

  • Cesarean Section
  • Anxiety
  • Postoperative Period

Keywords

  • Massage
  • cesarean delivery
  • anxiety
  • patient satisfaction
  • hemodynamic parameters
03

In context

Anxiety Disorders

5,063 studies on the registry are indexed under Anxiety Disorders; 1,408 are open to participants now.

This study's planned enrollment of 40 is below the median of 80 across 4,339 interventional studies indexed under Anxiety Disorders.

Browse Anxiety Disorders studies →

Lead sponsor

Dokuz Eylul University is the lead sponsor of 257 studies on the registry; 34 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
20 Years to 35 Years
Sexes eligible
Female
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Women aged between 20 and 35 years.
  • Underwent an elective term cesarean delivery.
  • Having a healthy newborn with a 1-minute Apgar score > 7.
  • Being at the 4th postoperative hour.
  • No diagnosed psychological disorders (such as depression or anxiety disorder).
  • Not using any anxiolytic medications.
  • Having no contraindications for hand massage (i.e., absence of skin lesions, burns, or musculoskeletal pathologies on the hands).

Exclusion criteria

Exclusion Criteria:

  • Development of severe postoperative complications (e.g., excessive bleeding, infection).
  • Conditions requiring admission to the Intensive Care Unit (ICU).
  • Presence of postnatal complications.
  • Having chronic or ongoing systemic diseases.
  • Having any skin lesions, burns, open wounds, or musculoskeletal pathologies on the hands.
  • Inability to speak and understand Turkish.
05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
40 participants (estimated)

Study arms

  • Experimental
    Reflexology Hand Massage

    A 20-minute reflexology hand massage applied by the researcher. Pressure is applied to specific reflex points on the hands to promote relaxation, reduce anxiety, and support hemodynamic stability.

    Other: Reflexology Hand Massage

  • Placebo comparator
    Stroking Hand Massage

    Participants in this group will receive a 20-minute stroking hand massage as a placebo intervention, applied at the 4th postoperative hour after elective cesarean delivery.

    Other: Stroking Hand Massage

Interventions

  • OtherReflexology 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.

  • OtherStroking 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.

06

What researchers measure

Primary outcomes

  1. Change in State Anxiety Levels

    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.

    Time frame: Baseline (before the intervention at the 4th postoperative hour) and 30 minutes after the completion of the 20-minute massage.

Secondary outcomes

  1. Change in Patient Satisfaction

    Patient satisfaction will be evaluated using a Visual Analog Scale (VAS). The scale is a 10-centimeter line ranging from 0 to 10, where 0 represents 'completely dissatisfied' and 10 represents 'completely satisfied.' Higher scores indicate greater satisfaction with the postoperative care.

    Time frame: Baseline (before the intervention at the 4th postoperative hour) and 30 minutes after the completion of the 20-minute massage.

  2. Change in Hemodynamic Parameters1

    Physiological evaluation will include the measurement of systolic blood pressure (mmHg), diastolic blood pressure (mmHg)

    Time frame: 1 Baseline (before the intervention at the 4th postoperative hour) and 30 minutes after the completion of the 20-minute massage.

  3. Change in Hemodynamic Parameters 2

    Physiological evaluation will include the measurement of heart rate (beats per minute)

    Time frame: 2 Baseline (before the intervention at the 4th postoperative hour) and 30 minutes after the completion of the 20-minute massage.

  4. Change in Hemodynamic Parameters 3

    Physiological evaluation will include the measurement of respiratory rate (breaths per minute)

    Time frame: 3 Baseline (before the intervention at the 4th postoperative hour) and 30 minutes after the completion of the 20-minute massage.

  5. Change in Hemodynamic Parameters 4

    Physiological evaluation will include the measurement of peripheral oxygen saturation (SpO2, %).

    Time frame: 4 Baseline (before the intervention at the 4th postoperative hour) and 30 minutes after the completion of the 20-minute massage.

07

Study locations

1 of 1 sites recruiting
  • Dokuz Eylul University Research and Application Hospital
    Izmir, 35340, Turkey (Türkiye)
    Recruiting
08

References and documents

Publications

  • 1. Abidi, S. M. A., Abbas, S., Abidi, S. T. F., Hussain, N., & Haresh, S. (2023). Application of the Robson classification in assessing cesarean section rates: An audit of a tertiary care hospital's gynecology department in Karachi, Pakistan. medRxiv. https://doi.org/10.1101/2023.04.30.23289336 2. World Health Organization. (2021). Caesarean section rates continue to rise, amid growing inequalities in access. https://www.who.int/news/item/16-06-2021-caesarean-section-rates-continue-to-rise-amid-growing-inequalities-in-access 3. Yang, J. (2025). Cesarean sections in selected countries 2022. Statista. 4. Uğuryol, M., & Dönmez, A. (2022). The effect of reflexology treatment on anxiety. Journal of Psychiatric Nursing, 13(1), 24-30. https://doi.org/10.14744/phd.2021.05579 5. Roshangar, F., Lotfi, M., Aghazadeh, A. M., Asghari, E., & Aghaei, E. (2020). The effect of "nurse companionship" on anxiety and vital sign changes of cesarean section candidates: A randomized control trial. Crescent Journal of Medical and Biological Sciences, 7(2), 267-273. 6. Kunikata H, Watanabe K, Miyoshi M, Tanioka T. The effects measurement of hand massage by the 7. autonomic activity and psychological indicators. Journal of Medical Investigation. 2012;59[1-2]:206-12 8. Aksu, S., & Karaca, P. P. (2021). The Effect of Reflexology on Lactation in Women Who Had Cesarean Section: A Randomized Controlled Pilot Study. Complementary Medicine Research, 28(4), 336-343. 9. Joseph, A., Frank, R. W., & Ramyashree, S. (2024). Postoperative Pain Reduction in "Cesarean Mothers" with Hand and Foot Massage. Journal of Health and Allied Sciences NU, 14(Suppl S1), S18-S20. 10. Kiliçli, A., & Zeyneloglu, S. (2024). Effect of Reflexology on Pain, Fatigue, Sleep Quality, and Lactation in Postpartum Primiparous Women After Cesarean Delivery: A Randomized Controlled Trial. Journal of Human Lactation, 40(2), 221-236. 11. Mahima, A., Saraswathy, K., Venkatesan, L., Vijayalakshmi, K., & Dhanalakshmi, V. (2025). Effective

Individual participant data

Plan to share: No

09

Updates

1 registry update since Sep 25, 2026
Registered
First appeared on the registry. No changes since
Oct 19, 2026
Show all 1 update
  1. Oct 19, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07880587
Responsible party
Buse Güler (Assistant Professor, Dokuz Eylul University) — Principal investigator
First posted
Oct 19, 2026
Start date
Jun 26, 2026
Primary completion
Jan 30, 2027 (estimated)
Completion
Jan 30, 2027 (estimated)
Last update
Oct 19, 2026

Study contacts

Buse Güler, PhD
Contact
busebahitli@gmail.com
+90 232 412 69 70
Gizem Göktuna
study director · Dokuz Eylul University
Erkan Çağlıyan
study director · Dokuz Eylul University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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