Comparative Effects of High-Intensity Interval Training and Continuous Endurance Training Among Prediabetic Patients

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age35-54
SponsorRiphah International University

About this trial

Prediabetics is a condition where blood sugar levels are normal but not yet high enough to be diagnosed as type 2 diabetes. This phase offers a crucial point for timely intervention to delay or prevent type 2 diabetes. The objective of the study will be to find the effects of high intensity interval and continuous endurance training on glycemic control, BMI, Vo2 Max, pulmonary function and physical activity among prediabetic patients. Study design will be randomized control trial. Total 80 participants will be enrolled in study. The data will be collected from faculty of Riphah International University, Lahore. The study will be completed within 8 months after approval of synopsis. A simple random sampling will be used to assign the groups; group A and group B. Group A will be assigned high intensity interval training and group B will be assigned to continuous training.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Sedentary lifestyle (Individuals reporting minimal structured physical activity e.g., <30 minutes of exercise per week) .

Stable Medical Condition (No history of significant cardiovascular events, uncontrolled hypertension, or other major comorbidities).

Stable Body Weight (Stable body weight with changes less than 3 kg in the past 6 months).

Disqualifiers

uncontrolled hypertension

history of heart disease

myocardial infarction

stroke

Trial design

Design model

Parallel

Treatments tested in this trial

  • High-Intensity Interval Training

    Behavioral

    5 minutes warm up including walk * 30s fast stairs climbing * 60s slow walk down * Repeat 5 to 6 rounds * 5 minute stretching or slow walk (cool down)

  • Continuous Endurance Training

    Behavioral

    5 to 10 minute walking (warm up ) * 25 to 30minutes at 60 to 70 %continuous training * Continuous walk for 15 to 20 minutes. * 5 to 10 minutes stretching (cool down)

Treatment groups

80 Participants
are divided into 2 treatment groups
Group A: High-Intensity Interval TrainingActive comparator 1 intervention
Group B: Continuous Endurance TrainingActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

fasting blood glucose

Participants were instructed to fast overnight for 8 to 12 hours. FBG was measured using an automated glucose analyzer

Time frame
12 weeks
2

Forced Vital Capacity

Spirometry using devices like a digital spirometry will be used. Forced Vital Capacity (FVC) will be measured in liters (L) using spirometry. FVC represents the maximum volume of air that can be forcefully exhaled after a maximal inspiration.

Time frame
12 weeks
3

Forced Expiratory Volume in One Second

Forced Expiratory Volume in One Second (FEV₁) will be measured in liters (L) using spirometry. FEV₁ represents the volume of air exhaled during the first second of a forced expiratory maneuver.

Time frame
12 weeks
4

FEV₁/FVC ratio

The FEV₁/FVC ratio will be expressed as a percentage (%) and calculated from spirometric measurements to assess the degree of airflow limitation.

Time frame
12 weeks

Secondary outcomes

1

Body mass index (BMI)

Participants weight was measured using a calibrated digital scale with minimal clothing and no shoes height was measured using a wall mounted stadiometer with participants standing upright

Time frame
12 weeks
2

IPAQ (short form) questionnaire

International physical activity questionnaire is applicable for survey among 18 to 65 years to Assess the level of physical activity along different countries. It is developed in 2 Versions; first is long version (27 items), and the second is the short version (7 items). We will use IPAQ short version which consists of job, transport, domestic, and leisure time physical activity domains. Moderate and high-intensity walking and sitting time activities are addressed in this questionnaire

Time frame
12 weeks
3

Maximal Oxygen Uptake (VO₂max)

In this research VO2 Max will be measured through a submaximal 6 mint walk test

Time frame
12 weeks

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.