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Clinical Trials/NCT04267666
NCT04267666
Completed
Not Applicable

Comparative Study of Inspiratory Muscle Strength Training and Incentive Spirometer on Ventilatory Function in Postmenopausal Asthmatic Women

Cairo University1 site in 1 country40 target enrollmentJuly 1, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Asthmatic
Sponsor
Cairo University
Enrollment
40
Locations
1
Primary Endpoint
MVV (Maximum voluntary ventilation)
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

Objective: To compare the effectiveness of inspiratory muscle training (IMT) and incentive spirometer on ventilatory functions in post-menopausal asthmatic women. Participants and methods: A total of forty postmenopausal women suffering from asthma, their ages ranged from 50 to 60 years old, and their body mass index of the patient don't exceed 30kg/m2. They were recruited from patient chest clinic in Kasr -El- Ainy Teaching Hospital, Cairo University, Egypt.

Detailed Description

They signed a consent form, confidentiality was assured. They assigned into two groups (A) who received inspiratory muscle training in the form of: Inspiratory threshold muscle trainer in addition to traditional chest physical therapy intervention (Deep breath, cough training) while patients in group (B): received traditional chest physical therapy intervention and incentive spirometer, three sessions per week for six weeks. Patients in both groups were assessed before treatment (pre-training) then after treatment (post-training) (after 6 weeks) to measure lung functions using electronic spirometer. The training program was carried in the duration from January 2019 to July 2019.

Registry
clinicaltrials.gov
Start Date
July 1, 2019
End Date
December 30, 2019
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Ghada Ebrahim El Refaye

assistant professor Department of Physical Therapy for Women's Health, Faculty of Physical therapy, Cairo University, Egypt

Cairo University

Eligibility Criteria

Inclusion Criteria

  • Forty postmenopausal women suffering from asthma
  • Their ages were ranged from 50 to 60 years,
  • their body mass index (BMI) don't exceed 30kg/m
  • All participants were asthmatic patient
  • clinically and medically stable cases

Exclusion Criteria

  • participant who had chest infection,
  • malignant diseases,
  • Patients with chest trauma.

Outcomes

Primary Outcomes

MVV (Maximum voluntary ventilation)

Time Frame: 6 weeks

is the maximum air, which can be expired in a minute by deepest and fastest breathing, reported as a number in liters (L)

Electronic Spirometer (VIASYS- Health Care Microlab)

Time Frame: 6 weeks

It was used for ventilatory functions measurement Ventilatory,reported as a number in liters (L).

FVC (Forced vital capacity)

Time Frame: 6 weeks

is one of the most useful tests to assess the overall ability to move air in and out of the lungs (ventilation). This is the maximum amount of air that can be forcefully and rapidly exhaled after a deep breath (maximal inspiration),reported as a number in liters (L)

FEV1 (Forced expiratory volume)

Time Frame: 6 weeks

is the volume of air forcibly exhaled in one second during the FVC test,reported as a number in liters (L)

Secondary Outcomes

  • Body mass index(6 weeks)

Study Sites (1)

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