The Effect of Endorphin Massage Applied to Postpartum Women on Anxiety and Fatigue Levels
NCT ID: NCT06421233
Last Updated: 2024-05-20
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
50 participants
INTERVENTIONAL
2023-09-04
2023-11-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Endorphin Massage Application to Women Who Gave Birth Vaginally
NCT05764512
The Effect of Back Massage Applied to Mothers in the Early Postpartum Period on Parameters
NCT06200649
Investigation of the Effect of Massage Application on Functional Status and Depression in Postpartum Mothers
NCT06539858
Effects of Back Massage After Cesarean Section
NCT06162156
Does Endorphin Massage Reduce the Anxiety of Pregnant Women?
NCT06342154
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
DOUBLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Intervention group
* Personal introduction form, state and trait anxiety scale and visual similarity scale for fatigue were applied.
* Endorphin massage was applied twice by the researcher for 15 minutes every two hours.
* After the endorphin massage applied for the second time, the visual similarity scale and the state and trait anxiety scale were applied again for fatigue.
massage
Endorphin massage will be given for 15 minutes every 2 hours.
Control gruop
* A personal introduction form, state and trait anxiety scale, and visual similarity scale for fatigue were applied.
* Two hours after the first evaluation, the visual similarity scale and the state and trait anxiety scale were applied again for fatigue.
No interventions assigned to this group
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
massage
Endorphin massage will be given for 15 minutes every 2 hours.
Other Intervention Names
Discover alternative or legacy names that may be used to describe the listed interventions across different sources.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Postpartum within 24 hours,
* Primiparous,
* Those who are healthy and have given birth to a single baby,
* Postpartum women who volunteered to participate in the study were included.
Exclusion Criteria
* People with chronic diseases (Heart disease, Thyroid problems, Diabetes mellitus, Hypertension, asthma, COPD,
* Those who have been diagnosed with a risky pregnancy (Pre-eclampsia, Arthritis, Pregnancy-related hypertension, Gestational diabetes),
* Whose baby was admitted to neonatal intensive care,
* Postpartum women with postpartum bleeding were not included in the study.
19 Years
40 Years
FEMALE
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
TC Erciyes University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Nurseli Soylu Erener
Research Assistant
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Nurseli SOYLU ERENER
Role: PRINCIPAL_INVESTIGATOR
TC Erciyes University
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Kayseri City Hospital
Kocasinan, Kayseri, Turkey (Türkiye)
Countries
Review the countries where the study has at least one active or historical site.
Related Links
Access external resources that provide additional context or updates about the study.
Qian, J., Sun, S., Liu, L., \& Yu, X. (2021). Protocol: Effectiveness of non-pharmacological interventions for reducing postpartum fatigue: a systematic review protocol. BMJ Open, 11(10), 51136
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
2023/516
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.