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Clinical Trials/NCT06098638
NCT06098638
Completed
Not Applicable

Effect of Aerobic and Resisted Exercise on Lipid Profile and Quality of Life in Overweight Breastfeeding Women: A Randomized Clinical Trial

Cairo University1 site in 1 country54 target enrollmentStarted: January 1, 2023Last updated:

Overview

Phase
Not Applicable
Status
Completed
Enrollment
54
Locations
1
Primary Endpoint
measurement of lipid parameter level of High-density lipoprotein (HDL) mg/dL

Overview

Brief Summary

the aim of the study was to investigate the effect of aerobic and resisted exercise program on lipid profile and quality of life in overweight breastfeeding women.

Detailed Description

Although previous studies reported that exercise training during the postpartum period could improve the lipid profile and quality of life in overweight women and reduce the postpartum fatigue . None of them had investigated the effect of aerobic and resisted exercises on lipid profile and quality of life in overweight breastfeeding women.this trial will include 2 groups:

Group (A): was consist of 27 overweight breastfeeding women, who received nutritional recommendation and faradic current stimulation for 20 min on abdominal surface 2 times per week for 12 weeks.

Group (B): was consist of 27 overweight breastfeeding women, who received the same nutritional recommendation and faradic current stimulation for 20 min on abdominal surface 2 times per week plus exercise training (aerobic + resisted) for 12 weeks.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Double (Participant, Outcomes Assessor)

Masking Description

double (participant, outcomes Assessor)

Eligibility Criteria

Ages
20 Years to 30 Years (Adult)
Sex
Female
Accepts Healthy Volunteers
No

Inclusion Criteria

  • All of women were sedentary, non-smoking, breastfeeding women at their 3rd to 6th months postpartum
  • they had delivered a single, healthy, mature fetus with no complications through normal vaginal delivery.
  • Their age was ranged from 20 to 30 years old.
  • Their parity number was one or two.
  • They were overweight (body mass index (BMI) was ranged from 25 to 30 kg/m²).

Exclusion Criteria

  • Having chronic disorders, heart disease, respiratory infections, diabetes mellitus, pelvic abnormalities, hormonal abnormalities, psychological problems, menstrual disorders or anemia of other pathological origins.
  • Receiving any type of physical exercise or sport.
  • Following a specific diet program.

Outcomes

Primary Outcomes

measurement of lipid parameter level of High-density lipoprotein (HDL) mg/dL

Time Frame: 12 weeks

It was used to measure the lipid profile parameters (High-density lipoprotein (HDL)- level in for each woman in the both groups (A \& B) at pre-treatment and post-treatment.

measurement of Triglycerides (TG) mg/dL

Time Frame: 12 weeks

t was used to measure the lipid profile parameters Triglycerides (TG) level for each woman in the both groups (A \& B) at pre-treatment and post-treatment.

measurement of Low-density lipoprotein (LDL) mg/dL

Time Frame: 12 weeks

It was used to measure the lipid profile parameters Low-density lipoprotein (LDL) level for each woman in the both groups (A \& B) at pre-treatment and post-treatment.

Secondary Outcomes

  • calculation of score of Short Form 36 Health Survey Questionnaire (SF-36) (Arabic version):(12 weeks)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Marwa Gamal Mohamed Ali

physical therapist at Abo Kabir general hospital

Cairo University

Study Sites (1)

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