Effects of Interrupting Prolonged Sitting With Different Standing Intervals on Vascular Health in Women
1 other identifier
interventional
24
1 country
1
Brief Summary
The goal of this clinical trial is to examine the effects of interrupting prolonged sitting with different standing intervals on vascular health in healthy women aged 18-45 years. The main questions it aims to answer are: Does interrupting prolonged sitting with short standing intervals (10 minutes every hour) improve blood pressure and pulse wave velocity more than prolonged continuous standing intervals (30 minutes every hour)? Does interrupting prolonged sitting with prolonged intermittent standing intervals (30 minutes every hour divided into three 10-minute standing bouts) improve blood pressure and pulse wave velocity more than prolonged continuous standing intervals (30 minutes every hour)? The researcher will compare three different sitting interruption conditions to evaluate their effects on vascular health outcomes: Standing for 10 minutes every hour. Continuous standing for 30 minutes every hour. Intermittent standing for 30 minutes every hour divided into three 10-minute standing bouts. Participants will: Attend three experimental sessions in random order separated by at least 7 days. Complete 3 hours of sitting with different standing interruption protocols. Undergo measurements of blood pressure, pulse wave velocity, and heart rate before sitting and after each hour of the experiment. Undergo height, weight, and body mass index measurements.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Apr 2026
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
April 2, 2026
CompletedFirst Submitted
Initial submission to the registry
August 31, 2026
CompletedFirst Posted
Study publicly available on registry
September 3, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 20, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
October 10, 2026
ExpectedSeptember 3, 2026
May 1, 2026
6 months
August 31, 2026
August 31, 2026
Conditions
Outcome Measures
Primary Outcomes (3)
Blood Pressure
Systolic and diastolic blood pressure will be measured before sitting and after each hour during the experimental sessions.
Baseline, 1 hour, 2 hours, and 3 hours
Pulse Wave Velocity
Baseline, 1 hour, 2 hours, and 3 hours
Heart Rate
Baseline, 1 hour, 2 hours, and 3 hours
Study Arms (3)
Short Standing Interval
EXPERIMENTALParticipants will complete 3 hours of sitting interrupted with 10 minutes of standing every hour.
Continuous Standing Interval
EXPERIMENTALParticipants will complete 3 hours of sitting interrupted with 30 continuous minutes of standing every hour.
Intermittent Standing Interval
EXPERIMENTALParticipants will complete 3 hours of sitting interrupted with 30 minutes of standing every hour divided into three 10-minute standing bouts.
Interventions
Participants will interrupt prolonged sitting with 30 continuous minutes of standing every hour during 3 hours of sitting.
Participants will interrupt prolonged sitting with 30 minutes of standing every hour divided into three 10-minute standing bouts during 3 hours of sitting.
Participants will interrupt prolonged sitting with 10 minutes of standing every hour during 3 hours of sitting.
Eligibility Criteria
You may qualify if:
- Female participants aged 18-45 years. Healthy individuals with normal blood pressure levels (systolic blood pressure \<130 mmHg and diastolic blood pressure \<80 mmHg).
- Body mass index (BMI) less than 30 kg/m². Ability to stand without support. No history of cardiovascular disease or chronic diseases that may affect study outcomes.
You may not qualify if:
- Pregnancy or breastfeeding. Back injuries preventing prolonged sitting. Use of medications that may affect cardiovascular responses, including antihypertensive, antidiabetic, antidepressant, or hormonal medications.
- Presence of chronic diseases or cardiovascular conditions affecting vascular health.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
King Saud University
Riyadh, Saudi Arabia
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
Abdullah B Alansare, PhD
King Saud University
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- BASIC SCIENCE
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Physical Education Teacher and Master's Student
Study Record Dates
First Submitted
August 31, 2026
First Posted
September 3, 2026
Study Start
April 2, 2026
Primary Completion
September 20, 2026
Study Completion (Estimated)
October 10, 2026
Last Updated
September 3, 2026
Record last verified: 2026-05