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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03467321
Other study ID # 2017/176
Secondary ID
Status Completed
Phase N/A
First received March 5, 2018
Last updated March 9, 2018
Start date August 1, 2017
Est. completion date December 29, 2017

Study information

Verified date March 2018
Source Ataturk Training and Research Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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.


Recruitment information / eligibility

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

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Physical characteristic assessment
Physical characteristics related to balance, pulmonary function and low back pain were evaluated

Locations

Country Name City State
Turkey Ankara Yildirim Beyazit University Ankara

Sponsors (1)

Lead Sponsor Collaborator
Seyda TOPRAK CELENAY

Country where clinical trial is conducted

Turkey, 

Outcome

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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