Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05949437
Other study ID # P.T.REC/012/004556
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date July 17, 2023
Est. completion date December 30, 2023

Study information

Verified date July 2023
Source October 6 University
Contact Ali MA Ismail, Phd
Phone 01005154209
Email ali.mohamed@pt.cu.edu.eg
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Is there effect of yoga breathing exercises versus aerobic exercise on hematological parameters in iron deficiency anemic females? The purpose of the study is to investigate the effect of yoga breathing exercises versus aerobic exercise on hematological parameters in iron deficiency anemic females


Description:

60 patients with iron deficiency anemia and will receive medical treatment of anemia and Dietary advice for 12 weeks . thirty patient from the 60 patients will receive yoga therapy and 50 minutes yoga therapy 6 days a week for 12 weeks while the other 30 patients will receive aerobic exercise for 12 weeks


Recruitment information / eligibility

Status Recruiting
Enrollment 60
Est. completion date December 30, 2023
Est. primary completion date December 1, 2023
Accepts healthy volunteers No
Gender Female
Age group 30 Years to 40 Years
Eligibility Inclusion Criteria: 1. Sixty female patients referred with iron deficiency anemia 2. Their age will be ranged from 30-40 years old. 3. All patients have a history of anemia. 4. All patients should be medically stable. 5. The body mass index (BMI) ranged from 25:29.9 Kg/m2 6. Number of parity not exceed 3 times. 7. Period of menses from 3-5 days Exclusion Criteria: 1. Patients with cognitive impairments. 2. All types of anemia except iron deficiency anemia 3. patients with hearing problems. 4. patients with Diabetes, Hypertension. 5. Patients with Musculoskeletal, Neurological, Cardiovascular and Respiratory problems 6. patients with mental problems.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Yuga
Traditional yoga body posture for 15 minutes, yoga breathing exercises for 30 minutes and meditation for 5 minutes for 12 weeks
Aerobic exercises
in form of treadmill according to the target exercise heart rate for 12 weeks

Locations

Country Name City State
Egypt October 6 university Giza

Sponsors (1)

Lead Sponsor Collaborator
Shokry Mahmoud Youssef Mohamed

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary serum iron level it will be measured in serum from complete blood picture. Reference range from 50 till 212 ug/dl. Number of participants are 60 females. it will be measured after 12 weeks
Primary ferritin level it will be measured in serum from iron profile. Reference range from 10 till 158 ng/ml. Number of participants are 60 females. it will be measured after 12 weeks
Primary iron binding capacity level it will be measured in serum from iron profile. Reference range from 250 till 400 ug/dl. Number of participants are 60 females. it will be measured after 12 weeks
Primary count of red blood cells it will be measured in serum from complete blood picture. Reference range from 3.80 till 4.80 million cell/cmm. Number of participants are 60 females. it will be measured after 12 weeks
Primary Hemoglobin level it will be measured in serum from complete blood . picture. Reference range from 12 till 15 g/dl. Number of participants are 60 females. it will be measured after 12 weeks
Primary hematocrite level it will be measured in serum from complete blood picture. Reference range from 36% till 45%. Number of participants are 60 females. it will be measured after 12 weeks
Primary lymphocytes level it will be measured in serum from differential white cell count. Reference range absolute from 1000 till 4000 and relative from 20% till 45%. Number of participants are 60 females. it will be measured after 12 weeks
Secondary six minute walking distance The six minute walking distance is measured using six Minute Walk Test which is a sub-maximal exercise test used to assess aerobic capacity and endurance. The distance covered over a time of 6 minutes is used as the outcome by which to compare changes in performance capacity.
The tools are used include 30 meters corridor,2 cones,stopwatch,chair,mechanical lap counter and sphygmomanometer Number of participants are 60 females.
it will be measured after 12 weeks
Secondary The fatigue severity scale(FSS) The FSS questionnaire contains nine statements that rate the severity of your fatigue symptoms. Read each statement and circle a number from 1 to 7, based on how accurately it reflects your condition during the past week and the extent to which you agree or disagree that the statement applies to you.
A total score of less than 36 suggests that you may not be suffering from fatigue.
A total score of 36 or more suggests that you may need further evaluation by a physician.
Number of participants are 60 females.
it will be measured after 12 weeks
See also
  Status Clinical Trial Phase
Recruiting NCT06027801 - Iron Fortified Food to Improve Japanese Encephalitis and Typhoid Fever Vaccine Immunogenicity N/A
Completed NCT02282553 - Gastric Capsule Examination for Iron Deficiency Anaemia N/A
Recruiting NCT05217836 - Iron Metabolism Disorders in Patients With Sepsis or Septic Shock.
Recruiting NCT04913649 - Intravenous Iron to Treat Postoperative Anemia in Older Cardiac Surgery Patients Phase 4
Completed NCT02176759 - Iron Absorption From Rice Fortified With Ferric Pyrophosphate N/A
Completed NCT01438645 - ScopeGuide-assisted Colonoscopy Versus Conventional Colonoscopy N/A
Completed NCT01307007 - Hypophosphatemia With Ferric Carboxymaltose Vs. Iron Dextran in Iron Deficiency Secondary to Heavy Uterine Bleeding Phase 2
Completed NCT00982007 - Efficacy and Safety of Intravenous Ferric Carboxymaltose (FCM) in Patients With Iron Deficiency Anemia (IDA) Phase 3
Completed NCT00198848 - Iron Supplementation Among Adolescent Girls in India N/A
Completed NCT01166451 - The Anemia Control Program: High or Low Iron Supplementation N/A
Recruiting NCT03893045 - A Study to Evaluate Ferumoxytol for the Treatment of Iron Deficiency Anemia (IDA) in Pediatric Subjects Phase 3
Recruiting NCT03817957 - Postoperative i.v. Iron Substitution in Patients With Diagnosed Iron Deficiency Phase 3
Completed NCT03819530 - Child of Urban Poverty Iron Project (CUPIP) - A Pilot Study N/A
Completed NCT03618914 - Anemia and Inflammation
Completed NCT03940430 - Lactoferrin Versus Ferrous Sulfate in Management of Iron Deficiency Anemia Among Female Medical Ain Shams Students Phase 2/Phase 3
Withdrawn NCT03873584 - Improvement of Fatigue Symptoms in the Iron Deficiency Anemia With Iron Succinylate Therapy
Enrolling by invitation NCT03897673 - Optimizing Benefits While Reducing Risks of Iron in Malaria-endemic Areas N/A
Active, not recruiting NCT04778072 - A Clinical Study on Adherence and Efficacy of Different Doses of Active Iron in Treatment Resistant Subjects N/A
Completed NCT03237065 - Incidence of Hypophosphatemia After Treatment With Iron Isomaltoside/Ferric Derisomaltose or Ferric Carboxymaltose in Subjects With Iron Deficiency Anaemia Phase 3
Completed NCT05153278 - IV Iron Versus Standard Treatment for Iron Deficiency Anemia in the Emergency Department