Menu
Recruiting NCT07730879

How Wall Squat Exercise Affects Blood Pressure in People With High Blood Pressure and Treated Sleep Apnea (WALLPRESS)

No phase Interventional Hypertension Obstructive Sleep Apnea (OSA)

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Isometric Wall Squat.
Who it may be relevant to
Registry conditions: Hypertension, Obstructive Sleep Apnea (OSA). Basic parameters: 18 years — 80 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Portugal
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

Acute Blood Pressure Responses to Isometric Wall Squat Exercise in Adults With Hypertension and CPAP-Treated Obstructive Sleep Apnea: A Randomized Crossover Trial

Overview

This study will look at whether a simple exercise called the isometric wall squat can help lower blood pressure in adults who have both hypertension and obstructive sleep apnoea treated with CPAP. Obstructive sleep apnoea is a condition in which breathing repeatedly stops or becomes shallow during sleep, and it is closely linked to high blood pressure. Although CPAP helps treat sleep apnoea, it usually lowers blood pressure only a little, so additional non-drug strategies may be useful. The study will compare two situations in the same participants: one session of wall squat exercise and one non-exercise control session. Each participant will take part in both sessions, but the order will be random. This design helps the researchers compare blood pressure changes more fairly within the same person. Participants will first attend a familiarization session, where the study procedures will be explained and the exercise intensity will be checked. After that, they will complete the two study sessions at home, during their usual CPAP treatment visits. The sessions will be separated by at least 48 hours and completed within one week. Both sessions will be scheduled at the same time of day to reduce the effect of normal daily changes in blood pressure. The main result the researchers will measure is the average systolic blood pressure during the 12 hours after each session, using ambulatory blood pressure monitoring. This means blood pressure will be measured over time while the participant goes about normal daily activities. The researchers want to find out whether a single session of wall squat exercise produces a greater blood pressure reduction than simply resting without exercise. This study may help improve understanding of whether isometric exercise can be a practical, low-cost, home-based option to support blood pressure control in people with hypertension and CPAP-treated obstructive sleep apnoea.

Interventions

  • Other Isometric Wall Squat
    4x2-min isometric wall squat contractions separated by 2-min rest periods plus standard drug therapy

Primary outcome measures

  • 12-hour systolic blood pressure [Time frame: During the 12 hours following the exercise or control session]
Secondary outcome measures (3)
  • 12-hour diastolic blood pressure [Time frame: During the 12 hours following the exercise or control session]
  • Short-term blood pressure variability [Time frame: During the 12 hours following the exercise or control session]
  • Pulse pressure [Time frame: During the 12 hours following the exercise or control session]

Eligibility criteria

Inclusion criteria

  • 18-80 years old.
  • Diagnosis of hypertension and OSA confirmed by polysomnography or respiratory sleep study.
  • Apnea-Hypopnea Index (AHI) of at least 15 events per hour.
  • Treatment with CPAP for at least 3 months.

Exclusion criteria

  • Mean CPAP adherence <4 hours/night over the last month, documented by device download.
  • Heart failure.
  • Peripheral artery disease.
  • Atrial fibrillation.
  • Chronic obstructive pulmonary disease.
  • Chronic kidney disease.
  • History of acute coronary syndrome, stroke, or transient ischemic attack in the previous 12 months.
  • Relevant changes in antihypertensive or other cardiovascular pharmacotherapy in the previous 3 months.
  • Relevant changes in CPAP prescription in the previous 3 months.
  • Any contraindication to exercise according to contemporary ESC/ACSM recommendations (e.g. unstable angina).
  • Pregnancy or breastfeeding.
  • Neurological and/or orthopaedic conditions that could interfere with exercise (e.g. severe knee osteoarthritis, recent lower-limb surgery).
  • Inability to read, understand, or provide informed consent.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Crossover
Masking
Open label
Primary purpose
Treatment

Study locations

Portugal · 1 center
  • Nippon Sanso Homecare — Braga

Identifiers

NCT: NCT07730879 · 153-CEIC-UA/2026-M

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗