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Optimal Frequency of High-Intensity Interval Training for Centrally Obese Adults

The University of Hong Kong (HKU) logo

The University of Hong Kong (HKU)

Status

Completed

Conditions

Obesity

Treatments

Other: Usual Care
Behavioral: Thrice-Weekly HIIT
Behavioral: Once-Weekly HIIT

Study type

Interventional

Funder types

Other

Identifiers

NCT04887454
1v3HIIT

Details and patient eligibility

About

The aim of this study is to examine the therapeutic effectiveness of two different exercise frequencies of high-intensity interval training (HIIT; once versus thrice weekly, with matched weekly exercise volume) on improving cardiometabolic risk factors in centrally obese adults.

Full description

HIIT is an emerging, popular, promising, cost-effective, and time-efficient exercise modality for managing obesity. Although lower-frequency HIIT is favorable for intervention adherence, the optimal exercise frequency of HIIT for alleviating obesity is unknown.

This study is a three-arm randomized controlled trial. Centrally obese adults will be randomly allocated to three groups: the usual care control, once and thrice-weekly HIIT groups. Led by research personnel, the usual care group will receive obesity-related health education. Led by athletic coaches, the HIIT intervention groups will receive 16 weeks of once or thrice weekly HIIT (with matched weekly exercise volume). Outcome measures of this study will be examined at baseline, 4 months (post-intervention), and 8 months (follow-up), by assessors blinded to group allocation.

Enrollment

315 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Aged above 18 years
  • Ethnic Chinese
  • Overweight (BMI ≥23 for Asian)
  • Centrally obese according to IDF and NCEP with Asian-specific cut-off (waist circumference ≥90 cm for males; ≥80 cm for females)
  • Males and females

Exclusion criteria

  • Medical and somatic conditions that prevent brisk walking
  • Chronic diseases affecting mobility and motor function (e.g., neurological disease, musculoskeletal disorder, spinal cord injury, autoimmune, arthritis, Parkinson's Disease)
  • Chronic diseases affecting cardiorespiratory and metabolic health (e.g., cancers, cardio-/cerebrovascular diseases, heart disease, diabetes mellitus, pneumonia, chronic pulmonary diseases, nephritis, nephrosis)
  • Signs of cardiac arrhythmia indicated by aberrant electrocardiography during incremental VO2max test
  • Regular moderate-to-vigorous intensity exercise (≥150 min weekly) in the past 3 months, as screened by a specially designed questionnaire
  • Daily smoking habit
  • Excess alcohol consumption (daily ≥30g for men, ≥20g for women) in the past six months
  • Claustrophobia
  • Surgery, therapy or medication for obesity or weight loss in the past six months (e.g., gastric bypass, gastric band, sleeve gastrectomy, gastric reduction duodenal switch, and dietitian-prescribed dietary program)

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

315 participants in 3 patient groups

Once-Weekly HIIT
Experimental group
Description:
Once-weekly HIIT for 16 weeks, led by certified athletic coaches
Treatment:
Behavioral: Once-Weekly HIIT
Thrice-Weekly HIIT
Experimental group
Description:
Thrice-weekly HIIT for 16 weeks, led by certified athletic coaches
Treatment:
Behavioral: Thrice-Weekly HIIT
Usual Care
Other group
Description:
Bi-weekly health education, led by research personnel
Treatment:
Other: Usual Care

Trial contacts and locations

1

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Central trial contact

Parco M. Siu, PhD

Data sourced from clinicaltrials.gov

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