Effects Of Moderate Physical Activity On Hb, Physical Fitness And Psychological Well Being In Females

January 24, 2022 updated by: Riphah International University
The study is design To determine the effectiveness of moderate physical activity on Hb, Physical fitness and psychological well-being in females.

Study Overview

Status

Completed

Conditions

Detailed Description

The majority of literature showed that level of physical activity is associated with Hb level. But there is paucity in the literature regarding the cause and effect relationship of PA and Hb. Literature shows lacking that there is any defined physical activity, which can affect the Hb concentration. According to literature, different studies conduct at Hb level in individuals with different diseases i.e. rheumatic arthritis, Diabetes mellitus etc. The aim of my study is to determining the cause and effect relationship of moderate physical activity on Hb level in healthy female population, one of the easiest moderate physical activity is brisk walk. Brisk walk is an aerobic exercise. People do get best physiological results of aerobic exercise with intensity of exercise 60-70% of the maximum pulse with longer time duration as well as increase frequency of exercise, which increase no of hemoglobin level due to this need more oxygen to performing physical activity in return basal metabolic rate increases and achieve physical fitness and gain relieve from the psychological problems.

Study Type

Interventional

Enrollment (Actual)

22

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Pakistan/Federal
      • Islamabad, Pakistan/Federal, Pakistan, 44000
        • Pakistan

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 25 years (ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

Female

Description

Inclusion Criteria:

1. Female 2.18-25 years 3. Hb<12

Exclusion Criteria:

  1. Lower limb musculoskeletal injury
  2. Any head Injury or trauma in past 6 months.
  3. Any neurological or musculoskeletal condition
  4. Acute or chronic infections diseases

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: OTHER
  • Allocation: RANDOMIZED
  • Interventional Model: PARALLEL
  • Masking: SINGLE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: Interventional group
  1. Warm up and cool down
  2. Brisk walk (30 mintues each session per week 5 days)
  3. Week 1 to 6
  1. Warm up and cool down
  2. Brisk walk (30 mintues each session per week 5 days)
  3. Week 1 to 6
Other Names:
  • Moderate physical activity
NO_INTERVENTION: Control group
Routine activity

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Hemoglobin level concentration
Time Frame: 6 week
Hemoglobin is a protein in red blood cells that carries iron. In adults,In study hemoglobin level will be measured in healthy females which will be less than 12.
6 week
Physical activity readiness questionnaire (PAR-Q)
Time Frame: 6 week
The Physical Activity Readiness Questionnaire (PAR-Q) is a common method of uncovering health and lifestyle issues prior to an exercise programme starting. The questionnaire is short and easy to administer and reveals any family history of illness.
6 week
Physical Fitness Test ( 12-minute run test)
Time Frame: 6 week
The 12-minute run fitness test as an easy way to measure aerobic fitness .The Cooper 12-minute run test requires the person being tested to run or walk as far as possible in a 12-minute period. The objective of the test is to measure the maximum distance covered by the individual during the 12-minute period
6 week
Physical Fitness Test( Shuttle run test)
Time Frame: 6 weeks
Shuttle Run is a test of agility, in which the participant runs back and forth between two parallel lines as fast as possible.
6 weeks
Physical Fitness Test(Sit and reach test)
Time Frame: 6 weeks
The sit and reach test is a common measure of flexibility, and specifically measures the flexibility of the lower back and hamstring muscles.
6 weeks
Physical fitness test(lateral plyometric test)
Time Frame: 6 weeks
Lateral plyometric jumps are advanced exercises that can be used to develop power and agility
6 weeks
Physical fitness test(Push-ups)
Time Frame: 6 weeks
The upper body muscles that come into play in the pushup are the deltoids of the shoulders, the pectoral muscles of the chest, the triceps and biceps of the upper arm, and the erector spinae of the back.
6 weeks
Perceived stress scale (PSS)
Time Frame: 6 weeks
The Perceived Stress Scale (PSS) is the most widely used psychological instrument for measuring the perception of stress. It is a measure of the degree to which situations in one's life are appraised as stressful.
6 weeks
International physical activity Questionaire (IPAQ)
Time Frame: 6 weeks
We are interested in finding out about the kinds of physical activities that people do as part of their everyday lives. The questions will ask you about the time you spent being physically active in the last 7 days.
6 weeks
Quality of life SF-12 scale
Time Frame: 6 weeks
The SF-12 is a self-reported outcome measure assessing the impact of health on an individual's everyday life. It is often used as a quality of life measure.
6 weeks
VO2max
Time Frame: 6 weeks
V̇O₂ max is the maximum rate of oxygen consumption measured during incremental exercise; that is, exercise of increasing intensity. The name is derived from three abbreviations: "V̇" for volume, "O₂" for oxygen, and "max" for maximum.
6 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ACTUAL)

April 29, 2021

Primary Completion (ACTUAL)

December 10, 2021

Study Completion (ACTUAL)

December 30, 2021

Study Registration Dates

First Submitted

March 12, 2021

First Submitted That Met QC Criteria

September 20, 2021

First Posted (ACTUAL)

September 28, 2021

Study Record Updates

Last Update Posted (ACTUAL)

January 26, 2022

Last Update Submitted That Met QC Criteria

January 24, 2022

Last Verified

January 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • REC/00929 Rabbya Kausar

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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