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Hypertension, SystolicAPCIQ-BPNCT05903950

Air Pollution and Cardiovascular Disease in Qatar: an Interventional Study to Reduce Blood Pressure

A study testing Air cleaners with HEPA filter and Air cleaners without HEPA filter in people with Hypertension, Systolic and Metabolic Syndrome, run by Weill Cornell Medical College in Qatar at 1 site in Qatar.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record

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Trial summary

The main objective is to determine if in-home portable air cleaners provide persistent reductions in PM2.5 exposures and improvements in systolic blood pressure and biochemical parameters over one week in patients with metabolic syndrome or type 2 diabetes residing in Qatar. Read more about this study

Who is it for?
Ages 18 to 65 years
What is being tested?
Air cleaners with HEPA filter and Air cleaners without HEPA filter
Type of treatment
Medical device
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
100 participants
Where
1 siteQatar
Study dates
3 Nov 2024to Dec 2026
Phase
Interventional

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 65 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Age ≥18 and less than 65 years old
  • Living in a single residence (home, apartment) located anywhere in Qatar
  • Mild systolic hypertension: screening visit systolic BP 130 to 159 mm Hg (off treatment or taking ≤ 2 BP medications that have been stable without changes during prior one week)
  • Either:
  • Type 2 diabetes patients (HbA1c > 6.5%) OR Non-type 2 diabetes patients with two or more additional criteria for the metabolic syndrome,
  • Waist circumference ≥102 cm if male and ≥88 cm if female
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  • Fasting triglycerides ≥150 mg/dL (or taking a triglyceride-lowering medication)
  • HDL-C ≤ 40 mg/dL if male and ≤ 50 mg/dL if female (or taking an HDL-raising medication),
  • Fasting glucose ≥100 mg/dL (or taking an antidiabetic medication)

Who cannot join

  • Pregnancy (self-reported)
  • ≥stage 4 kidney disease (estimated glomerular filtration rate <30 ml/min).
  • A medical condition placing the participant at risk from participation (per investigators)
  • Expected overnight travel outside their residence during the study
  • HEPA filter within the ACs of the residence (self-reported) or individual use of HEPA filter filter
  • Unable to comprehend/sign an informed consent
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  • Lung disease requiring oxygen
  • Cancer receiving treatment.
  • Type 1 diabetes or MODY diabetes
  • Screening visit: BP ≥160/100 mm Hg
  • Medication changes in the past week. If participants are on medications for high BP or hyperlipidemia, they will need to have had stable therapy for at least one week with no planned changes during the study
  • Left upper arm circumference >17 inches as this will make BP levels inaccurate with the home monitor used
  • Acute illness or infectious symptoms within the prior 4 weeks.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Charbel Abi Khalil, MD contact

+974 4492 8484

cha2022@qatar-med.cornell.edu

Qatar1 site, 1 recruiting
  • Hamad Medical Corporation

    Doha

    Jassim Al-Suwaidi, MD, +974 4439 5354, jalsuwaidi@hamad.qa

    Charbel Abi Khalil, MD, PhD

    Recruiting

Other trials in Qatar

About this study

Official title: Air Pollution and Cardiovascular Disease in Qatar: an Interventional Study to Reduce Blood Pressure: the APCIQ-BP Trial

The main objective is to determine if in-home portable air cleaners provide persistent reductions in PM2.5 exposures and improvements in systolic blood pressure and biochemical parameters over one week in patients with metabolic syndrome or type 2 diabetes residing in Qatar.

Read the detailed description

Chronic cardio-metabolic diseases such as hypertension and diabetes contribute disproportionately to global morbidity and mortality and are increasing believed to have multiple environmental influences.

PM2.5 is the fifth leading risk factor for global mortality - largely due to cardiovascular disease (CVD). Reducing personal exposure to air pollution has shown promise in improving key cardiovascular risk factors (blood pressure and insulin resistance) in limited studies, but durability of these effects is not known. Personal air cleaners have been shown to decrease personal exposure to PM2.5 and reduce blood pressure in small studies and may serve as a pragmatic intervention in high-risk patients in whom air pollution is a strong contributor to cardiovascular health.

Being tested
Air cleaners with HEPA filter, Air cleaners without HEPA filter
Keywords
hypertension, metabolic syndrome, air pollution, Type 2 Diabetes
Medical subject headings
Isolated Systolic Hypertension, Metabolic Syndrome, Hypertension, Diabetes Mellitus, Type 2

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Air cleaners with HEPA filterDevice

    PM 2.5 exposure reduction using in home portable air cleaners fitted with HEPA filters

  • Air cleaners without HEPA filterDevice

    Simulation of PM 2.5 exposure reduction using in home portable air cleaners without HEPA filters.

Study groups in NCT05903950
Study groupRoleWhat they receive
Active modeActive comparatorIn home use of portable air cleaners with a High Efficiency Particulate Air (HEPA) filter for one week.
Receives: Device: Air cleaners with HEPA filter
Sham modeSham comparatorIn home use of portable air cleaners without a High Efficiency Particulate Air (HEPA) filter for one week.
Receives: Device: Air cleaners without HEPA filter

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change in Systolic Blood Pressure

    Mean change from baseline in systolic blood pressure

    Measured: week 1, week 3

Secondary outcomes (2)
  1. Change in Fasting Glycemia

    Mean change from baseline in fasting glycemia

    Measured: week 4, week 10

  2. Change in Insulin Resistance Index

    Mean change from baseline in Insulin Resistance Index

    Measured: week 4, week 10

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted15 Jun 2023
  2. Study start3 Nov 2024
  3. Primary completionDec 2026 (estimated)
  4. Study completionDec 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Prevention
Allocation
Randomised
Intervention model
Crossover
Masking
Triple blind
Who is masked
Participant, Investigator, Outcomes assessor
Enrolment
100 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05903950
Sponsor's protocol ID
22-00009
Acronym
APCIQ-BP
Status last verified
Oct 2026
First submitted
5 Jun 2023
Last updated
23 Oct 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: Individual participant data that underlie the results reported in the article, after de-identification (test, tables, figures, and appendices).

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