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NCT06574854Completed

Effects of Descending Stair Walking

Effects of Descending Stair Walking on Cardiometabolic Adaptations Among Obese, Untrained Women

Source: ClinicalTrials.gov · Last updated 5 Feb 2026

Brief summary (registry, in English)

The global rise in the prevalence of physical inactivity is major public health concern. Lifestyle-related activities, such as stairs walking, has important public health implications and may represent an alternative approach for those who have difficulty adhering to conventional exercise programs. This two-armed, parallel-group, randomized controlled trial (RCT) aims to assess and compare the effects between the descending stair walking (DSW) and ascending stair walking (ASW) on cardiometabolic health markers, cardiopulmonary capacity, body composition and muscular strength. This RCT will recruit 16 obese inactive and sedentary females will be randomized using permuted block randomization into two arms: intervention arm, DSW and active comparator arm: ASW in a 1:1 allocation ratio. The participants in the DSW and ASW arms will undergo twice a week stair walking intervention session for 8 weeks. The exercise volume will be gradually increased over 8 weeks by increasing the number of repetitions by two every week for both arms. Borg's scale of perceived exertion (RPE) and visual analogue scale (VAS) will be used to assess subjective intensity of stair walking and pain intensity immediately after each repetition. Assessments will be carried out through two time points, pre-intervention assessment (T0) and immediately after completion of the intervention at 8 weeks (T1). During each assessment, the primary outcome to be assessed includes the cardiometabolic health markers and cardiopulmonary capacity, while the secondary outcomes to be assessed are the body composition and muscular strength. Whereas during the intervention, continuous heart rate and gas consumption will be monitored at week 1 (W1), week 4 (W4) and week 8 (W8) to monitor the intensity of the exercise.

Status (registry)
Completed
Study type
Interventional
Enrollment
24 (actual)
First submitted
14 Aug 2024
Start date
1 May 2023
Primary completion date
1 Mar 2025
Lead sponsor
Universiti Sains Malaysia
Diseases
Obesity
NCT number
NCT06574854

What you commit to

  • Study type: Interventional
  • Participants enrolled: 24
  • From 1 May 2023 to the primary completion date, 1 Mar 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • taking supplements or medication known to affect REE (such as oral contraceptives),
  • suffer from alcohol or drug abuse and

Other illness

  • severe medical conditions affecting their physical or mental health

Other

  • smokers
  • individuals with implanted medical device
  • trying to conceive/ pregnant or breastfeeding

Who the study is looking for

  • Women
  • age 18-50-year-old
  • BMI 25.0 - 39.9 kg/m2,
  • body fat percentage \> 30%
  • no lower limb orthopaedic injuries
  • sedentary lifestyle (regular exercise \<1 h per week).

Age in the registry: 18 years to 50 years · Sex: Female · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Wellness Hub Timur Laut, Pulau Pinang
Coordinator of this site? Confirm its status
Ayer ItamMalaysiaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.