Effects of Resistive Diaphragmatic Training on Chronic Stroke

NCT ID: NCT04636658

Last Updated: 2020-11-19

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

20 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-02-15

Study Completion Date

2020-09-01

Brief Summary

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To determine the effects of resistive diaphragmatic training on pulmonary function of chronic stroke patients. And also assessing their compromised respiratory functions

Detailed Description

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This study is to examine the effects of Diaphragmatic breathing exercises with resistance and Digital spirometer training for improving pulmonary functions in chronic stroke patients. Diaphragmatic Resistance training is based on the same principal as for the any other Skeletal Muscle training. The selection of 20 subjects divided equally and placed into an experimental group and a control group and the interventions would applied three times per week for 4 weeks. In each session, both groups receive Digital spirometer training for 15 minutes. In addition, experimental group receive diaphragm breathing exercises with resistance for 30 minutes. Resistance is Applied through Different thera bands and then performing the Breathing Exercises. First of all resistance applied through yellow band(1-6 pounds of resistance) and then red, Green and black which give (4-18 Pounds of resistance) The patient is asked to breath in deeply and slowly while not to move upper chest .Weight increased weekly as per patient's tolerance. Further Digital spirometer training Perform to determine the Pulmonary Functions FVC,FEV1,FVC/FEV1,PEF,VC. in both Control and Experimental Groups

Conditions

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Stroke (CVA) or TIA

Keywords

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stroke resistive diaphragmatic training pulmonary function

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Investigators

Study Groups

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Incentive spirometer training

Incentive spirometer training

Group Type ACTIVE_COMPARATOR

Incentive spirometer training

Intervention Type OTHER

Incentive spirometer training 5 sessions a week, each session of 15 minutes, for 4 weeks

diaphragmatic resistance exercises

Incentive spirometer training with diaphragm breathing with resistance exercises. Resistance is applied through the different Thera bands and then performing the pursed lip breathing exercise. Resistance increased weekly as per tolerance by the patient

Group Type EXPERIMENTAL

diaphragmatic resistance exercises

Intervention Type OTHER

Incentive spirometer with diaphragmatic resistance exercises. Resistance is applied through the different Thera bands and then performing the pursed lip breathing exercise. Resistance increased weekly as per tolerance by the patient.

Digital spirometer training for 15 minutes. diaphragm breathing exercises with resistance for 30 minutes. 5 sessions a week, for 4 weeks

Interventions

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Incentive spirometer training

Incentive spirometer training 5 sessions a week, each session of 15 minutes, for 4 weeks

Intervention Type OTHER

diaphragmatic resistance exercises

Incentive spirometer with diaphragmatic resistance exercises. Resistance is applied through the different Thera bands and then performing the pursed lip breathing exercise. Resistance increased weekly as per tolerance by the patient.

Digital spirometer training for 15 minutes. diaphragm breathing exercises with resistance for 30 minutes. 5 sessions a week, for 4 weeks

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Age limit 40-50yrs both genders.
* Stroke patients with compromised pulmonary functions.
* Chronic stroke patients with impaired Breathing

Exclusion Criteria

* Patients having any systemic illness
* Patients who have a damage accompanying orthopedic disease such as thoracic deformation or rib fracture.
* Patients with stroke (less than 6 months duration)
Minimum Eligible Age

40 Years

Maximum Eligible Age

50 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Riphah International University

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Anam Aftab, Phd*

Role: PRINCIPAL_INVESTIGATOR

Riphah International University

Locations

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District Hospital Sargodha

Sargodha, Punjab Province, Pakistan

Site Status

Countries

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Pakistan

References

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Other Identifiers

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REC/00237 Bushra Mushtaq

Identifier Type: -

Identifier Source: org_study_id