Effect of Lower Limb Resistance Versus Endurance Training in Smokers

NCT ID: NCT06674174

Last Updated: 2024-11-05

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

60 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-07-01

Study Completion Date

2024-07-18

Brief Summary

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Patients was selected based on inclusion and exclusion criteria. Experimental group was treated with Resistance training while control group received endurance training. Data was collected by spirometry and International Physical activity questionnaire readings was recorded in every session for baseline, 3rd week and 6thweeks.

Detailed Description

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Experimental group will receive lower limb strength training and control group will receive endurance training. Both groups will receive treatment for three days a week and each session will be given according to FITT formula. Measurement will be recorder pre-treatment and post treatment of both groups at baseline, third , and 6 th week.

Conditions

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Smoking

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants

Study Groups

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lower limb strength training

Experimental group will receive lower limb strength training

Group Type EXPERIMENTAL

lower limb strength training

Intervention Type OTHER

Experimental group will receive lower limb strength training treatment for three days a week and each session will last for an hour for 3 consecutivemonths. Measurement will be recorder pre-treatment and post treatment of both groupsat baseline,3rd, and 6th week.

endurance training

control group will receive endurance training.

Group Type OTHER

endurance training

Intervention Type OTHER

Control group will receive endurance training, treatment for three days a week and each session will last for an hour for 3 consecutivemonths. Measurement will be recorder pre-treatment and post treatment of both groupsat baseline,3rd, and 6th week.

Interventions

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lower limb strength training

Experimental group will receive lower limb strength training treatment for three days a week and each session will last for an hour for 3 consecutivemonths. Measurement will be recorder pre-treatment and post treatment of both groupsat baseline,3rd, and 6th week.

Intervention Type OTHER

endurance training

Control group will receive endurance training, treatment for three days a week and each session will last for an hour for 3 consecutivemonths. Measurement will be recorder pre-treatment and post treatment of both groupsat baseline,3rd, and 6th week.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Young cigarette smokers (10 cigarette/day for at least 10 years)
* Male
* Age 25-45 years
* Sedentary lifestyle
* Body mass: less than 80kg
* BMI:22-30

Exclusion Criteria

* Heart or pulmonary disease
* MSK disorder
* incapable of realizing the protocol of exercises,
* Recent surgery
* Recent Trauma.
* Any infective respiratory illness.
Minimum Eligible Age

25 Years

Maximum Eligible Age

45 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

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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Maria Razzaq, MsCPPT

Role: PRINCIPAL_INVESTIGATOR

Riphah International University

Locations

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Samina International Hospital

Dera Ismāīl Khān, , Pakistan

Site Status

Countries

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Pakistan

Other Identifiers

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Masroor Alam

Identifier Type: -

Identifier Source: org_study_id

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