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Clinical Trials/NCT05710003
NCT05710003
Not yet recruiting
Not Applicable

Effect of Breathing Exercises and Upper Limb Endurance Exercises in Pregnant Women Presented With Physiological Dyspnea

Entsar Hsanen0 sites28 target enrollmentFebruary 1, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pregnancy Related
Sponsor
Entsar Hsanen
Enrollment
28
Primary Endpoint
Modified dyspnea Borg scale
Status
Not yet recruiting
Last Updated
3 years ago

Overview

Brief Summary

To evaluate the effects of breathing exercises and upper limb endurance exercises in pregnant women presented with physiological dyspnea

Detailed Description

Pregnant women undergo various anatomical and physiological changes so that they can cope with the increased physical and metabolic demands of their pregnancies. Cardiovascular, respiratory, haematological, renal, gastrointestinal and endocrine systems undergo important physiological adaptations needed to allow development of the fetus and to allow the mother and fetus to survive the demands of childbirth . On the other hand, dyspnea can be caused by pregnancy complications, thus requiring specific medical treatment. Shortness of breath is common during pregnancy, occurring in 60% to 70% of healthy pregnant women . The aim of the study is to evaluate the effects of breathing exercises and upper limb endurance exercises in pregnant women presented with physiological dyspnea

Registry
clinicaltrials.gov
Start Date
February 1, 2023
End Date
December 1, 2023
Last Updated
3 years ago
Study Type
Interventional
Study Design
Single Group
Sex
Female

Investigators

Sponsor
Entsar Hsanen
Responsible Party
Sponsor Investigator
Principal Investigator

Entsar Hsanen

doctor

Assiut University

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Modified dyspnea Borg scale

Time Frame: 4 weeks

Modified Borg Dyspnea Scale is most commonly used to assess symptoms of breathlessness. It has a range from 0 to 10 (with 0 being no exertion and 10 being maximum effort).

Secondary Outcomes

  • Modified Medical Research Council Dyspnea Scale (mMRC)(4 weeks)
  • London chest activity of Daily Living questionnaire (LCADL)(4 weeks)

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