Pregnancy Related Clinical Trial
Official title:
Assistant Professor, Physioterapist, PhD
Verified date | March 2018 |
Source | Ataturk Training and Research Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
The aims of this study were to investigate balance and pulmonary functions in pregnant and non-pregnant women and to determine their relationship with LBP.
Status | Completed |
Enrollment | 75 |
Est. completion date | December 29, 2017 |
Est. primary completion date | November 1, 2017 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 18 Years to 40 Years |
Eligibility |
Inclusion Criteria: - pregnant women (in the second and third trimester), non-pregnant women, aged between 18 and 40 years, volunteering to participate in the study Exclusion Criteria: - Having a high-risk pregnancy, preeclampsia, multiple pregnancies, gestational diabetes mellitus, hypertension, any physical disability, prior history of surgery related to spine or abdominal, spinal deformity, serious neurological, rheumatologic, cardiopulmonary or psychiatric diseases, malignancy, fracture history, or those having any exercise program or sportive activity in the last 3 months for pregnant women - Having any physical disability, spinal or abdominal surgery, spinal deformity, serious neurological, rheumatologic, cardiopulmonary or psychiatric diseases, malignancy, or fracture history, or those having any exercise program or sportive activity in the last 3 months for non-pregnant women |
Country | Name | City | State |
---|---|---|---|
Turkey | Ankara Yildirim Beyazit University | Ankara |
Lead Sponsor | Collaborator |
---|---|
Seyda TOPRAK CELENAY |
Turkey,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Balance | Balance with the one leg balance test was assessed | through study completion, an average of 6 months | |
Secondary | Pulmonary function | Pulmonary function with a spirometer was assessed | through study completion, an average of 6 months | |
Secondary | Low back pain | Low back pain with the Visual Analogue Scale was assessed | through study completion, an average of 6 months |
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