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Recruiting NCT06952348

NCT06952348 HYPERtension Reduction Through WALKing Stairs Versus Brisk Walking

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Clinical Trial Summary
NCT ID NCT06952348
Status Recruiting
Phase
Sponsor Karolinska Institutet
Condition Metabolic Disease
Study Type INTERVENTIONAL
Enrollment 450 participants
Start Date 2025-11-27
Primary Completion 2028-12

Eligibility & Interventions

Sex All sexes
Min Age 35 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Stair and brisk walking combinedBrisk walkingStandard care

Eligibility Fast-Check

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What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 450 participants in total. It began in 2025-11-27 with a primary completion date of 2028-12.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This clinical trial investigates whether incorporating stair walking into daily routines improves physical health in adults at risk of lifestyle-related conditions such as hypertension, type 2 diabetes, and cardiovascular disease. Participants will be randomized into three groups: (1) stair walking combined with brisk walking, (2) brisk walking alone, and (3) a control group receiving standard lifestyle advice without specific exercise instructions, stratified by age (\<65 y/o, v \>=65) and site. The primary objective is to assess whether the combination of stair and brisk walking leads to greater reductions in systolic blood pressure compared to brisk walking alone or standard care. Secondary outcomes include changes in cardiometabolic risk factors. Participants in the stair walking group will be instructed to climb ≥250 steps per day (\~5.5 minutes/day or \~37.5 minutes/week), or complete an equivalent elevation via inclined slopes, along with ≥75 minutes of brisk walking per week. Those in the brisk walking group will walk ≥150 minutes per week. The control group will receive general lifestyle advice but no tailored physical activity goals or feedback. Participants in both active groups will aim to double their baseline activity levels. Physical activity will be continuously monitored using wearable devices. The active groups will receive personalized feedback and motivational support throughout the 6-month intervention period. If effective, this study may offer a simple, scalable, and low-cost intervention model for use in clinical and public health settings, emphasizing personalized goals, remote monitoring, and behavioral support.

Eligibility Criteria

Inclusion Criteria Men and women aged 35 years or older with increased cardiometabolic risk, defined by all of the following: 1. Clinically confirmed hypertension, with or without antihypertensive treatment, as documented in the Electronic Health Record (EHR). 2. Overweight or obesity, defined as BMI between 27 and 40. 3. Physically inactive lifestyle, defined as either: * Light intensity or inactive category on the Stanford Brief Activity Survey (SBAS), or * Light intensity or inactive category in the physical activity section of the Swedish National Board of Health and Welfare Lifestyle Questionnaire. Exclusion Criteria Medical contraindications to physical activity (based on FYSS 2021, p. 182): * Severe, symptomatic aortic stenosis * Acute pulmonary embolism, myocarditis, pericarditis, or systemic infection (e.g., fever, muscle pain, lymphadenopathy) * Suspected or known aortic dissection * Severe hypertension (Grade 3: SBP \>180 mmHg or DBP \>110 mmHg), regardless of symptoms * Unstable coronary artery disease (including unstable angina, suboptimally treated stable angina, or recent myocardial infarction \<8 weeks) * Symptomatic, uncontrolled arrhythmia * Symptomatic, uncontrolled heart failure Other exclusion criteria: * Implanted pacemaker or ICD * Pregnancy * Smartphone incompatibility with Fitrockr© app (iOS \<16 or Android OS \<10) * Inability to understand Swedish or English * Any condition that may interfere with protocol compliance (e.g., severe mental illness or cognitive impairment) * Inability to walk stairs

Contact & Investigator

Central Contact

Carl Johan Sundberg

✉ carl.j.sundberg@ki.se

📞 0046852480000

Frequently Asked Questions

Who can join the NCT06952348 clinical trial?

This trial is open to participants of all sexes, aged 35 Years or older, studying Metabolic Disease. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06952348 currently recruiting?

Yes, NCT06952348 is actively recruiting participants. Contact the research team at carl.j.sundberg@ki.se for enrollment information.

Where is the NCT06952348 trial being conducted?

This trial is being conducted at Stockholm, Sweden, Stockholm, Sweden, Stockholm, Sweden, Stockholm, Sweden.

Who is sponsoring the NCT06952348 clinical trial?

NCT06952348 is sponsored by Karolinska Institutet. The trial plans to enroll 450 participants.

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