- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06745752
Late Postpartum Period and Pain
Incidence, Severity, and Determinants of Upper Back, Lower Back, and Pelvic Girdle Pain in the Late Postpartum Period
Study Overview
Status
Conditions
Detailed Description
Research questions
- What are the prevalence rates of upper back, lower back, and pelvic girdle pain points during the 0-2 months postpartum period?
- What are the severity rates of upper back, lower back, and pelvic girdle pain points during the 0-2 months postpartum period?
- What are the determinants of upper back, lower back, and pelvic girdle pain points during the 0-2 months postpartum? The population of the study will consist of postpartum participants registered in a district family health center (FHC) in western Turkey, who meet the inclusion criteria and are willing to participate in the study. The total number of postpartum women registered in the family health center in the year before the study began was 383. Therefore, no sample calculation was made and all participants who gave birth within one year after the beginning of the study will be included in the study.
The data of the study will be collected using the Information Form, and Brief Pain Inventory.
Information Form: This form consists of 15 questions about sociodemographic and obstetric characteristics based on an extensive literature review on the topic.
Brief Pain Inventory: Developed by Cleeland and Ryan in 1994, the Pain Inventory consists of seven items related to pain intensity and the dimension of how pain interferes with daily activities.
Data collection The researcher will explain the purpose of the study to pregnant women who meet the inclusion criteria, invite them to participate, and obtain their consent. Data will be collected from participants at the end of the first postpartum week (when they attend the first postpartum follow-up visit and newborn heel prick test), at the end of the first month (day 28) (when they attend the second dose of neonatal hepatitis B vaccine), and at the end of the second month (week 8 postpartum) (when they attend the first dose of BCG, DTP-Hib-HBV, and IPV vaccines). At the first visit, participants will complete an information form and the Brief Pain Inventory. At the second and third meetings, they will complete only the Brief Pain Inventory.
Statistical analysis Statistical analysis will be performed using IBM SPSS Statistics 29.0 software (IBM Corp., Armonk, NY, USA). Sociodemographic data will be evaluated using descriptive statistical methods (frequency, percentage, mean, standard deviation). Kolmogorov-Smirnov test will be used as normality test. Independent samples analysis, correlation analysis and logistic regression analysis will be used in the analyses. Significance will be accepted as p<0.05.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Kocaeli, Turkey, 41380
- Kocaeli University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Participants who were 0-2 months postpartum,
- Could read and speak Turkish,
- Between the ages of 18-49.
Exclusion Criteria:
- Participants with past or current mental illness,
- Those taking antidepressant or anxiolytic medications,
- Rheumatoid arthritis,
- Ankylosing spondylitis,
- Scheuermann disease,
- Ehlers-danlos syndrome,
- Spinal surgery,
- Nerve root compression,
- Spondylolisthesis,
- Perineal edema,
- Hematoma,
- Wound dehiscence,
- Bladder catheterization,
- serious postpartum complications (internal bleeding, femoral artery embolism, pelvic fracture),
- Those whose babies are in the neonatal intensive care unit,
- Those who left the research unfinished.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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postpartum women
In the study, the upper back, lower back and pelvic girdle pain status of the participants in the postpartum period will be monitored.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Evaluation of upper back pain, lower back pain, and pelvic girdle pain
Time Frame: Postpartum day 7.
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Filling out the tools used in the research (Information Form and Brief Pain Inventory)
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Postpartum day 7.
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Evaluation of upper back pain, lower back pain, and pelvic girdle pain
Time Frame: Postpartum day 28.
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Filling out the tools used in the research (Information Form and Brief Pain Inventory)
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Postpartum day 28.
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Evaluation of upper back pain, lower back pain, and pelvic girdle pain
Time Frame: Postpartum day 56.
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Filling out the tools used in the research (Information Form and Brief Pain Inventory)
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Postpartum day 56.
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- sdilek12
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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