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.
RECRUITING
NA
90 participants
INTERVENTIONAL
2024-10-08
2025-10-30
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.
Neurolinguistic Programming, Progressive Muscle Relaxation Exercises, and Breastfeeding
NCT06070792
Investigation of the Effect of Massage Application on Functional Status and Depression in Postpartum Mothers
NCT06539858
Effects of Laughter Therapy on Postpartum Mothers' Stress, Sleep, and Breastfeeding
NCT06851286
The Effect of Endorphin Massage Applied to Postpartum Women on Anxiety and Fatigue Levels
NCT06421233
The Effect of Breastfeeding Counseling Based on Motivational Interviewing
NCT06362876
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
When the literature was examined, no study was found that examined the effects of mindfulness-based stress reduction programme and neurolinguistic programme on fatigue, sleep quality, lactation and depression in the postpartum long term.
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
OTHER
QUADRUPLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Mindfulness-based stress reduction program
MBSR; Mindfulness-based stress reduction program. 8 weeks of practice once a week for 20 minutes each. Mindfulness-based stress reduction practices will be carried out online. Mothers will actively participate.
MBSR
20 minutes once a week for 8 weeks
Neurolinguistic programming
NLP; Neurolinguistic programming 8 weeks of practice once a week for 20 minutes each. Neurolinguistic programming will be carried out online. Mothers will actively participate.
NLP
NLP Neurolinguistic programming, 20 minutes once a week for 8 weeks
control
control; MBSR and NLP applications will not be performed. Mothers will be monitored online every week.
control
control group, no practice,
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
MBSR
20 minutes once a week for 8 weeks
NLP
NLP Neurolinguistic programming, 20 minutes once a week for 8 weeks
control
control group, no practice,
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
* caesarean section
* primiparous
* breastfeeding women
Exclusion Criteria
19 Years
35 Years
FEMALE
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Aysegul Kilicli
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Aysegul Kilicli
Gaziantep University Health Sciences Institute, Department of Nursing PhD.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
AYŞEGÜL KILIÇLI, Dr.
Role: STUDY_DIRECTOR
Muş Alparslan University
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Şanlıurfa training and research hospital
Sanliurfa, Eyalet/Yerleşke, Turkey (Türkiye)
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
Mauniv
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.