High Intensity Interval Training

10

Review clinical trials related to High Intensity Interval Training. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Effect of High Intensity Interval Training on Strength, Endurance and Flexibility

Strength and endurance are essential components for physical fitness of any individual. High intensity interval training provides time efficient benefits for strength and endurance training. Physical Therapy professionals and students need physical fitness for effective clinical performance of patients. There is limited research regarding physical performance of physical therapists itself

Participants needed: 66
Trial details
Age: 18-24Biological sex: AllType: InterventionalSponsor: University of Health Sciences LahoreUpdated: Jun 16, 2026Locations: 2
Eligibility criteria

Undergraduate physical therapy students aged 18-24 years. [+2]

Students with musculoskeletal pain and injuries. [+6]

Status: Not yet recruiting

The Effects of High-Intensity Interval Training on Gait, Balance, and Cognitive Functions in Individuals With Multiple Sclerosis

This study aims to comparatively investigate the effects of low-volume High-Intensity Interval Training (HIIT) versus Moderate-Intensity Continuous Training (MICT) on gait, balance, cognitive functions, and neurovascular biomarkers (BDNF, VEGF) in individuals with Multiple Sclerosis (MS). This randomized controlled trial will be conducted at Hacettepe University, Faculty of Physical Therapy and Rehabilitation.

Participants needed: 40
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Hacettepe UniversityUpdated: May 20, 2026Locations: 1
Eligibility criteria

Diagnosed with Multiple Sclerosis by a neurologist (Hacettepe University Hospita... [+5]

Status: Not yet recruiting

The Feasibility of LVHIIT on Inpatient Stroke Rehab

The objective of this study is to explore the safety and feasibility of conducting low-volume, high-intensity interval training (HIIT) on a total body recumbent stepper (TBRS) in persons with stroke in an inpatient rehabilitation setting.

Participants needed: 15
Trial details
Phase: Early Phase 1Age: 18-85Biological sex: AllType: InterventionalSponsor: University of Kansas Medical CenterUpdated: Apr 15, 2026
Eligibility criteria

-Both sexes between the age of 18-85 years at time of consent [+4]

Implanted pacemaker or defibrillator limiting exercise performance [+12]

Status: Not yet recruiting

Investigation of the Effects of High-Intensity Interval Exercise and Moderate-Intensity Continuous Exercise on Limb Volume, Functional Capacity, and Quality of Life in Patients With Lipedema

This randomized controlled clinical study aims to investigate and compare the effects of high-intensity interval training (HIIT) and moderate-intensity continuous training (MICT), when combined with intermittent pneumatic compression (IPC) therapy, on limb volume, functional capacity, pain, fatigue, anxiety, depression, sleep quality, and quality of life in women with lipedema. Lipedema is a chronic, progressive adipose tissue disorder primarily affecting women, characterized by abnormal and symmetrical fat accumulation in the lower extremities that does not improve with weight loss or limb elevation. It is often misdiagnosed as obesity or lymphedema, leading to delayed treatment. Lipedema causes pain, swelling, bruising, mobility limitation, and reduced quality of life. Conservative treatment options include compression therapy, manual lymphatic drainage, and exercise. IPC is a non-invasive treatment used to reduce limb volume and pain while improving function and quality of life. Exercise is also a cornerstone of conservative management, but the optimal exercise intensity for lipedema remains unclear. In this study, 69 female patients aged 18-65 years diagnosed with lipedema according to Halk and Damstra criteria will be randomly assigned into three groups: IPC + Home-based walking program IPC + High-Intensity Interval Training (HIIT) IPC + Moderate-Intensity Continuous Training (MICT) All participants will receive 15 IPC sessions (3 times per week for 5 weeks). The exercise programs (HIIT or MICT) will continue for 10 weeks, supervised by a physiotherapist. The home-based group will be encouraged to walk ≥10,000 steps daily using a pedometer application. Primary outcome: Change in limb volume measured by circumferential measurements and the truncated cone formula. Secondary outcomes: Pain (VAS), functional capacity (6-Minute Walk Test), muscle strength (dynamometry), pressure pain threshold (algometry), physical activity (IPAQ-SF), lower extremity function (LEFS), quality of life (SF-12), sleep quality (PSQI), fatigue (FSS), and anxiety/depression (HADS). Measurements will be taken at baseline (T0), after 15 IPC sessions (T1), and after 30 total sessions or 10 weeks (T2). The investigators hypothesize that both HIIT and MICT combined with IPC will provide superior improvements in physical and psychological outcomes compared to IPC with a home-based walking program alone.

Participants needed: 69
Trial details
Age: 18-65Biological sex: FemaleType: InterventionalSponsor: Marmara UniversityUpdated: Jan 6, 2026Locations: 1
Eligibility criteria

Female participants aged 18-65 years [+2]

Pregnancy or breastfeeding [+5]

Status: Recruiting

Effects of HIIT vs. TRE on Type 2 Diabetes Risk

The primary aim of this randomized controlled trial is to examine the effects of a 4-week high-intensity interval training (HIIT) and time-restricted eating (TRE) intervention on cardiometabolic biomarkers in adolescents and young adults.

Participants needed: 40
Trial details
Age: 14-30Biological sex: AllType: InterventionalSponsor: Syracuse UniversityUpdated: Oct 10, 2025Locations: 1
Eligibility criteria

Adolescents (age 14-17 years old with sex- and race-specific BMI percentile ≥85t...

Chronic medical conditions: heart disease, arrhythmias, diabetes, thyroid diseas... [+2]

Status: Recruiting

HIIT Effects on Cardiometabolic Health

The primary aim of this randomized clinical trial is to compare the effects of three different HIIT protocols and a control group on cardiometabolic health in young adults with obesity. Participants will be randomly assigned to one of the following three groups, with each having varying work-to-rest ratios: 1) HIIT-A, 2) HIIT-B, 3) HIIT-C, and 4) control group. HIIT-A, HIIT-B, and HIIT-C groups will participate in six sessions of a running based HIIT program over a 2-week training period. Pre-clinical markers of cardiovascular disease, blood lipids and fasting glucose will be measured at the following three time points: baseline, post-intervention, and 2 weeks after the training cessation (i.e., measure for detraining effect). All measurements will be performed three days before the training program and three days after the intervention to avoid the effect of the last training session. Afterwards, the detraining test will be measured 2 weeks post intervention.

Participants needed: 60
Trial details
Age: 18-25Biological sex: AllType: InterventionalSponsor: Syracuse UniversityUpdated: Jul 23, 2025Locations: 1
Eligibility criteria

Young adults with obesity (Age 18 to 25 years old, BMI ≥ 30 kg/m2).

Syndromic obesity; 1) Any clinical symptoms including cognitive delay, 2) abnorm... [+6]

Status: Recruiting

Optimizing Aerobic Fitness in Older Adults

Hospitalization and treatment for cardiovascular disease is one of the main contributors to disability in older adults. Moderate intensity continuous aerobic and resistance training have been the cornerstone of cardiac rehabilitation (CR) for decades to remediate hospital-acquired functional deficits, but some groups receive less or minimal functional benefit from this training. The proposed studies seek to optimize recovery of aerobic fitness and physical function among older cardiac patients using a novel high intensity training regimen with the long-term goal of reducing subsequent disability and improving clinical outcomes.

Participants needed: 114
Trial details
Age: 65+Biological sex: AllType: InterventionalSponsor: University of Vermont Medical CenterUpdated: Jun 8, 2025Locations: 1
Eligibility criteria

>65 years old [+2]

have an active malignancy (excluding non-melanoma skin cancer or low grade prost... [+2]

Status: Recruiting

HIIT in Sedentary Obese Adults: Effects on Metabolic Risk, Body Composition, and FABP4

It is aimed to investigate the responses of Fatty Acid Binding Protein 4 (FABP4), which has been discovered as a novel biomarker of obesity and metabolic diseases, to regular exercise training. The aim of this study is to investigate the effects of high-intensity interval training (HIIT) on cardiometabolic risk factors, body composition, and plasma FABP4 levels in sedentary obese adults.

Participants needed: 28
Trial details
Age: 20-35Biological sex: AllType: InterventionalSponsor: Eastern Mediterranean UniversityUpdated: May 15, 2025Locations: 1
Eligibility criteria

Aged between 20 and 35 years, [+4]

BMI > 35, [+8]

Status: Recruiting

Can Exercise Ameliorate Immunosenescence and Thereby Reduce Relapse in Head and Neck Cancer Patients

Through the implementation of this three-year project, investigators expect to find a safe and effective exercise prescription for patients with oral cancer after surgery. The findings will encourage and promise and add further support to the concept that exercise prescription is worth implementation as part of care for the patients with head and neck cancer.

Participants needed: 180
Trial details
Age: 20-80Biological sex: AllType: InterventionalSponsor: Chang Gung Memorial HospitalUpdated: Feb 28, 2025Locations: 1
Eligibility criteria

Age ≥20 [+4]

ECOG PS≥2 [+4]

Status: Recruiting

Effects of Upper Extremity Low Volume HIIT in Heart Failure

This study was planned to investigate the effects of upper extremity low-volume high-intensity interval training (LV-HIIT) on physical and cognitive function in patients with heart failure with preserved ejection fraction(HFpEF).The research was planned as a randomized controlled trial. Patients with clinically stable HFpEF at cardiology clinic will be included in the study. These cases will be randomly divided into two groups: intervention group and control grup. After 8 weeks intervention physical functions before and after treatment; functional exercise capacity, arm exercise capacities , peripheral muscle strength , fatigue cognitive functions; anxiety and depression and fear of movement will be evaluated.

Participants needed: 30
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Tarsus UniversityUpdated: Jan 3, 2025Locations: 2
Eligibility criteria

Clinical condition stable for ≥4 weeks. [+2]

Unstable angina pectoris [+13]