- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06539858
Investigation of the Effect of Massage Application on Functional Status and Depression in Postpartum Mothers
December 12, 2025 updated by: ZEYNEP İCLAL SAG, University of Yalova
Investigation of the Effect of Massage Application on Functional Status and Depression in Mothers in the Early Postpartum Period
Postpartum depression is a condition with high morbidity in mothers and negatively affects all family relationships.
It has been observed that depression in the mother at only 2 months of age negatively affects the relationship between the baby and the mother, and that mothers who are depressed and therefore their babies feel more negatively.
Symptoms usually start to appear from the 2nd or 3rd week after birth.
At the same time, most people focus on the physical characteristics of the mother after birth, such as her reproductive system, while ignoring her full functionality.
Full functionality is a multidimensional concept that includes personal care, baby care, family care, social and professional activities.
In the first weeks after discharge, the functional status of the mother may differ as a result of the roles she assumes at home.
Since the breastfeeding period will begin in new mothers, different treatment methods are preferred instead of drug treatment, one of which is massage therapy.
It is thought that massage therapy relaxes the muscles and changes psychological factors.
Previous studies conducted on postpartum women show that massage has a positive and healing effect on mothers.
While previous studies frequently mention its effects on depression, it has also been observed that there are few studies mentioning its functional status.
In light of this information, the aim of this study is to investigate the effects of massage on functional status and depression in postpartum women.
For this purpose, there will be 2 groups randomized as intervention and control groups.
The intervention will be performed as a 45-minute massage once a week for 4 weeks.
Data will be collected before the first intervention and after the last intervention.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Actual)
28
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Yalova, Turkey (Türkiye)
- University of Yalova
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Probability Sample
Study Population
Young mothers who had just given birth and met the inclusion criteria for the study
Description
Inclusion Criteria:
- Being within the first 6 months postpartum
Exclusion Criteria:
- Having a health condition that prevents lying face down (having stitches from a cesarean section, hypertension, etc.)
- Not being cooperative
- All conditions that contraindicate massage
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Interventional group
This group will receive massage once a week for 4 weeks.
|
General back massage from the base of the neck to the sacrum.
Classical massage techniques such as stroking and kneeding will be applied.
To be performed by a specialist physiotherapist.
|
|
non-intervention group
No intervention will be made to this group
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
depression
Time Frame: 4 weeks
|
will be evaluated with the internationally accepted Edinburgh Postpartum Depression Scale. the name of the scale we use Edinburgh Postpartum Depression Scale.
As the score obtained from this scale increases, the person's depression level also increases.
|
4 weeks
|
|
functionality
Time Frame: 4 weeks
|
The change in functionality will be evaluated using the postpartum functional status inventory.
Inventory of Functional Status After Childbirth Turkish was used.
According to this scale, a decrease in the score indicates that the functional status also decreases.
|
4 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
May 10, 2024
Primary Completion (Actual)
August 30, 2024
Study Completion (Actual)
March 30, 2025
Study Registration Dates
First Submitted
August 1, 2024
First Submitted That Met QC Criteria
August 1, 2024
First Posted (Actual)
August 6, 2024
Study Record Updates
Last Update Posted (Actual)
December 19, 2025
Last Update Submitted That Met QC Criteria
December 12, 2025
Last Verified
December 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Urogenital Diseases
- Mental Disorders
- Female Urogenital Diseases and Pregnancy Complications
- Pregnancy Complications
- Mood Disorders
- Puerperal Disorders
- Depressive Disorder
- Depression, Postpartum
- Therapeutics
- Complementary Therapies
- Physical Therapy Modalities
- Rehabilitation
- Therapy, Soft Tissue
- Musculoskeletal Manipulations
- Massage
Other Study ID Numbers
- 2024/3
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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