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CompletedNCT06834256vs(versus)Updated Feb 19, 2025

Intermittent Fasting vs. High-intensity Interval Training on the Lipid Profile of Obese Individuals.

An interventional study of intermittent fasting and low volume high intensity interval training in Obesity, sponsored by Cairo University. Completed at 1 site in Egypt. Open to participants aged 35 Years to 50 Years. Per ClinicalTrials.gov, last updated 2025-02-19.

Sponsored by Cairo University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 1 year 7 months after the study started (first participant enrolled Jul 2023, registered Feb 2025).
Phase
Not applicable
Study type
Interventional
Enrollment
80
Allocation
Randomized
Ages
35 Years to 50 Years
Sex
All
01

Study summary

we aimed to ascertain the effect of intermittent fasting (IF) vs. high-intensity interval training (HIIT) on the lipid profile and waist circumference (WC) of obese individuals.

Read the detailed description

Subjects and Methods: This study included 40 obese individuals of both genders aged 35-50 years with an abnormal lipid profile. The patients were allocated at random to either Group A or B, with both groups receiving medical treatment. Group A followed the IF regime, while Group B performed HIIT on the treadmill three times weekly, with an intervention duration of six weeks for both groups. Body mass index (BMI), WC, levels of total cholesterol (TC), triglyceride (TG), low-density lipoprotein (LDL), high-density lipoprotein (HDL), alongside the Framingham risk score (FRS) were the evaluated variables.

02

Conditions studied

  • Obesity

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Keywords

  • Intermittent Fasting,High-Intensity Training,,Obesity
03

In context

Obesity

6,297 studies on the registry are indexed under Obesity; 1,693 are open to participants now.

This study's enrollment of 80 is close to the median of 78 across 4,879 interventional studies indexed under Obesity.

Browse Obesity studies →

Lead sponsor

Cairo University is the lead sponsor of 4,780 studies on the registry; 1,427 are open to participants now.

Of its 36 completed or terminated interventional studies of FDA-regulated products, 5 (14%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
35 Years to 50 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

Inclusion criteria were as follows: (1) A BMI of 30 -40 kg/m2; (2) abnormal lipid profile, with a TC level > 200 mg/dL, an LDL > 100 mg/dL, a TC level > 150 mg/dL, and an HDL \< 40 mg/dL; (3) steady vital signs, including blood pressure, respiration rate, and temperature at a baseline level.

Exclusion criteria

Exclusion Criteria:

  • The exclusion criteria included patients with the following medical conditions: cancer, unstable angina, uncontrolled cardiac rhythm, decompensated heart failure, persistent systolic blood pressure > 200 mmHg, persistent diastolic blood pressure > 120 mmHg, acute pericarditis or myocarditis, severe restrictive lung disease, chronic chest infection, severe obstructive lung disease, pregnant women, neurological disorders that affect balance and mentality (e.g., epilepsy), orthopedic or neurological problems that interfere with exercises, unstable endocrinal disorders, congenital or acquired lower limb deformity, kidney disease, infectious disease, immune disease, hearing impairment or mental disorder, uncontrolled T2DM.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
80 participants (actual)

Study arms

  • Experimental
    Group A (IF group)

    Group A followed the intermittent fasting( IF) regime ,with an intervention duration of six weeks for both groups

    Behavioral: intermittent fasting

  • Experimental
    Group B performed High-intensity interval training( HIIT)

    High-intensity interval training performed on the treadmill three times weekly, with an intervention duration of six weeks for both groups

    Behavioral: low volume high intensity interval training

Interventions

  • Behavioralintermittent fasting

    Group A participants followed the IF diet for 6 weeks . intermittent fasting , specifically time-restricted feeding (TRF), involves consuming all of one's energy requirements inside an 8-h.The fasting interval was designated as 16 h, and the other 8-h was the eating period . During the 8-h eating window, the patient consumes a well-balanced meal consisting of 55%-65% carbs, 7%-20% protein, and 15%-30% fat .

  • Behaviorallow volume high intensity interval training

    . Group B engaged in low-volume HIIT exercise (aerobic activity) three times weekly for six weeks. The exercise routine consisted of a 5-min warm-up phase at 70% of MHR, followed by four intervals of 2-min maximum effort cycling sessions (4 × 2 HIIT) compared to a sub-maximal workload at 85%-90% of MHR. The participants engaged in four work bouts, with each bout lasting around 4 min and followed by a 4-min rest period. During the workouts, the participants maintained an HR of 60%-70% of their MHR. This resulted in 8 min of intense physical activity during each training session. Additionally, there was a 5-min cooling down phase at 70% of the MHR. The treatment's intensity was adapted based on the modified Bruce protocol.

06

What researchers measure

Primary outcomes

  1. lipid profile

    A 5 mL fasting venous blood sample was collected following an eight-hour overnight fast, and LDL, HDL, TG, and TC levels were measured.

    Time frame: lipid profile will be measured at baseline, and it will be measured again after six weeks

Secondary outcomes

  1. waist circumference

    Utilizing tape measurements to measure WC.A WC \> 40 inches (102 cm) in males and \> 35 inches (88 cm) in women indicated an elevated risk for cardiometabolic disorders

    Time frame: waist circumference will be measured at baseline, and it will be measured again after six weeks

  2. The Framingham risk score (FRS)

    It was employed to ascertain the cardiovascular disease risk over ten years.

    Time frame: The Framingham risk score (FRS) will be measured at baseline, and it will be measured again after six weeks

07

Study locations

1 site
  • Cairo University
    Cairo, Egypt
08

References and documents

Publications

  • Nussbaumerova B, Rosolova H. Obesity and Dyslipidemia. Curr Atheroscler Rep. 2023 Dec;25(12):947-955. doi: 10.1007/s11883-023-01167-2. Epub 2023 Nov 18. PubMed 37979064 ↗
  • Nazari M, Minasian V, Hovsepian S. Effects of Two Types of Moderate- and High-Intensity Interval Training on Serum Salusin-alpha and Salusin-beta Levels and Lipid Profile in Women with Overweight/Obesity. Diabetes Metab Syndr Obes. 2020 Apr 24;13:1385-1390. doi: 10.2147/DMSO.S248476. eCollection 2020. PubMed 32425570 ↗
09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 19, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06834256
Lead sponsor
Cairo University
Responsible party
Heba Ahmed Mousa (lecturer of physical therapy, Cairo University) — Principal investigator
First posted
Feb 19, 2025
Start date
Jul 1, 2023
Primary completion
Mar 2, 2024
Completion
May 1, 2024
Last update
Feb 19, 2025

Study contacts

Heba Mousa, lecturer
principal investigator · Cairo University

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Feb 2025. You cannot join it, but the record below documents what was studied.

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