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CompletedNCT07867561BAM-CBUpdated Oct 9, 2026

Back Massage for Postpartum Fatigue and Maternity Blues After Cesarean Birth

An interventional study of Back Massage in Postpartum Fatigue and Maternity Blues, sponsored by Kocaeli University. Completed at 1 site in Turkey (Türkiye). Open to female participants aged 18 Years to 45 Years. Per ClinicalTrials.gov, last updated 2026-10-09.

Sponsored by Kocaeli University · Not applicable, Interventional, and Supportive care

From the registry’s dates

  • Registered 1 year 4 months after the study started (first participant enrolled May 2025, registered Oct 2026).
Updated Oct 9, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
80
Allocation
Randomized
Ages
18 Years to 45 Years
Sex
Female
01

Study summary

This randomized controlled trial evaluated the effects of back massage applied after elective cesarean birth on postpartum fatigue and maternity blues. Women were randomly assigned to either a back massage group or a control group. The intervention group received a 30-minute back massage after the first postoperative mobilization, while the control group received routine postpartum care only. Postpartum fatigue and maternity blues were assessed on the second postoperative day before discharge.

Read the detailed description

This study was conducted as a two-group, parallel, randomized controlled trial to evaluate the effects of back massage applied after elective cesarean birth on postpartum fatigue and maternity blues. The study included 80 women who underwent elective cesarean birth and met the eligibility criteria. Participants were randomly assigned in a 1:1 ratio to either the back massage group or the control group.

Women in the back massage group received routine postpartum care in addition to a 30-minute back massage. The massage was administered by the second author after the first mobilization at the sixth postoperative hour. Women in the control group received routine postpartum care only and did not receive any additional intervention.

Postpartum fatigue and maternity blues were assessed on the second postoperative day before hospital discharge. Postpartum fatigue was evaluated using the Postnatal Accumulated Fatigue Scale, and maternity blues was assessed using the Maternity Blues Scale. Sociodemographic and obstetric characteristics were collected using a Participant Information Form developed by the researchers.

The primary objective of the study was to determine whether back massage after elective cesarean birth reduces postpartum fatigue and maternity blues compared with routine postpartum care alone.

02

Conditions studied

  • Postpartum Fatigue
  • Maternity Blues

Keywords

  • Back Massage
  • Cesarean Birth
  • Postpartum Fatigue
  • Maternity Blues
  • Postpartum Care
  • Nonpharmacological Intervention
03

In context

Lead sponsor

Kocaeli University is the lead sponsor of 214 studies on the registry; 39 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years to 45 Years
Sexes eligible
Female
Accepts healthy volunteers
No

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 who underwent elective cesarean birth
  • Women with a single healthy newborn
  • Women who did not have a negative response to massage or touch interventions
  • Women with intact skin and tissue integrity in the back area where the massage was applied

Exclusion criteria

Exclusion Criteria:

  • Women with communication problems
  • Women who underwent cesarean birth under general anesthesia
  • Women diagnosed during pregnancy or birth with complications such as oligohydramnios, preeclampsia, heart disease, diabetes, or placenta previa
  • Women who developed postpartum complications such as hemorrhage or hypertension
  • Women whose newborn required admission to the neonatal intensive care unit
  • Women who received additional analgesic or narcotic medication other than the routine postoperative analgesic treatment
05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Investigator)
Enrollment
80 participants (actual)

Study arms

  • Experimental
    Back Massage Group

    Participants assigned to the Back Massage Group received routine postpartum care plus a 30-minute back massage. The massage was administered after the first mobilization at the sixth postoperative hour following elective cesarean birth. Postpartum fatigue and maternity blues were assessed on the second postoperative day before discharge.

    Behavioral: Back Massage

  • No intervention
    Control Group

    Participants assigned to the Control Group received the hospital's routine postpartum care only and did not receive any additional intervention. Postpartum fatigue and maternity blues were assessed on the second postoperative day before discharge.

Interventions

  • BehavioralBack Massage

    Participants in the Back Massage Group received a 30-minute back massage in addition to routine postpartum care. The massage was administered after the first mobilization at the sixth postoperative hour following elective cesarean birth. The intervention was delivered by the second researcher. Participants continued to receive the hospital's standard postpartum care throughout the study.

06

What researchers measure

Primary outcomes

  1. Postpartum Fatigue Assessed by the Postnatal Accumulated Fatigue Scale

    The Postnatal Accumulated Fatigue Scale consists of 13 items and three subscales. Total scores range from 0 to 39, with higher scores indicating greater postpartum fatigue.

    Time frame: 48 hours after cesarean birth

  2. Maternity Blues Assessed by the Maternity Blues Scale

    The Turkish version of the Maternity Blues Scale consists of 28 items and five subscales. Higher scores indicate higher levels of maternity blues.

    Time frame: 48 hours after cesarean birth

07

Study locations

1 site
  • Kocaeli University
    Kocaeli, Turkey (Türkiye)
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Ran from May 2025 to primary completion in May 2026, 12 months.

How these figures are worked out, and which studies are left out of them.

Registered
Oct 2, 2026
First posted
Oct 9, 2026
StartActual
May 10, 2025
Primary completionActual
May 10, 2026
CompletionActual
May 10, 2026
Last update
Oct 9, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Registered
First appeared on the registry. No changes since
Oct 9, 2026
Show all 1 update
  1. Oct 9, 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
NCT07867561
Lead sponsor
Kocaeli University
Responsible party
Sena Dilek Aksoy (Associate Professor, Department of Midwifery, Kocaeli University) — Principal investigator
First posted
Oct 9, 2026
Start date
May 10, 2025
Primary completion
May 10, 2026
Completion
May 10, 2026
Last update
Oct 9, 2026

Study contacts

Sena Dilek Aksoy, Ph.D.
principal investigator · Kocaeli 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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This study is completed, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.

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