Skip to main content
Clinical Trials/NCT03467321
NCT03467321
Completed
Not Applicable

Assistant Professor, Physioterapist, PhD

Seyda TOPRAK CELENAY1 site in 1 country75 target enrollmentAugust 1, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pregnancy Related
Sponsor
Seyda TOPRAK CELENAY
Enrollment
75
Locations
1
Primary Endpoint
Balance
Status
Completed
Last Updated
8 years ago

Overview

Brief 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.

Registry
clinicaltrials.gov
Start Date
August 1, 2017
End Date
December 29, 2017
Last Updated
8 years ago
Study Type
Observational
Sex
Female

Investigators

Sponsor
Seyda TOPRAK CELENAY
Responsible Party
Sponsor Investigator
Principal Investigator

Seyda TOPRAK CELENAY

Asist. Prof, PT, PhD

Ataturk Training and Research Hospital

Eligibility Criteria

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

Outcomes

Primary Outcomes

Balance

Time Frame: through study completion, an average of 6 months

Balance with the one leg balance test was assessed

Secondary Outcomes

  • Low back pain(through study completion, an average of 6 months)
  • Pulmonary function(through study completion, an average of 6 months)

Study Sites (1)

Loading locations...

Similar Trials