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Chronic DiseaseNCT05271864

Smart Watch, Heart Rate and So2 in Chronic Patients

An observational study of Chronic Disease, run by Umm Al-Qura University at 1 site in Saudi Arabia.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Background: Apple watch validity to measure the heart rate (HR) and oxygen saturation (Spo2) in healthy subjects has been investigated, but its accuracy and validity for patients with chronic non-communicable diseases such as diabetes mellites (DM), hyperlipidemia and hypertension (HTN) is still unclear. Read more about this study

Who is it for?
Ages 18 to 85 years
Conditions the study is for
Chronic Disease
What is being tested?
Apple Watch
Type of treatment
Medical device
How many people
41 participants
Where
1 siteSaudi Arabia
Study dates
1 Nov 2022to 30 Jul 2023
Phase
Observational
Are there results?
None posted in the registry

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 85 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Patients with diabetic mellites, hypertension and hyperlipidemia

Who may be able to join

  • eligible participants will be patients with chronic diseases as those with:
  • Stable diabetes mellitus type 1 or 2.
  • Hypertension but not more than 180 mm.Hg
  • Hyperlipidemia

Who cannot join

  • patients with :
  • Uncontrolled diabetes mellitus.
  • Uncontrolled hypertension.
  • Uncontrolled hyperlipidemia will be all excluded from the study.
  • Patient with other chronic diseases rather than that described in the inclusion criteria will be also excluded.

Trial locations and contacts

1 site in 1 country.

Saudi Arabia1 site
  • Umm Al-Qura medical center

    Al Makhwāh, Mecca Region, 21234

Other trials in Saudi Arabia

About this study

Official title: Accuracy of Apple Watch to Measure Cardiovascular Indices in Patients With Chronic Diseases: A Cross Sectional Study

Background: Apple watch validity to measure the heart rate (HR) and oxygen saturation (Spo2) in healthy subjects has been investigated, but its accuracy and validity for patients with chronic non-communicable diseases such as diabetes mellites (DM), hyperlipidemia and hypertension (HTN) is still unclear. Patients with chronic diseases as DM, HTN and hyperlipidemia who have hypoxemia are advised to continuously monitor their Spo2. Therefore, this study aims to investigate the accuracy of the Apple watch in measuring the Spo2 and heart rate in patients with chronic diseases.

Method: A cross sectional study will invite ninety-five patients with chronic diseases to participate in this study and the eligible participants will be allocated into three groups. The first group (Group-A) will include patients with the DM, the second group (Group-B) will include the patients with HTN and the third group will include patients with hyperlipidemia. All participants will use the apple watch to evaluate the Spo2 against the pulse oximeter at rest. The main outcome will be the Spo2 and heart rate that will be evaluated at rest and before and after exercise for 15 minutes using the Apple watch, Spo2 and Polar HR monitored using the pulse oximeter.

Read the detailed description

Introduction:

Assessment of the heart rate (HR) is an essential process to determine proper exercise training intensity. (1) Utilization of the 12-leads electrocardiogram (ECG) is considered most objective heart rate assessment procedure. Polar chest strap arises as an alternative to the ECG when it is not accessible to use it outside the laboratories. The Polar chest strap proved valid and reliable instrument when tested against the ECG in healthy subjects (2-4) and patients with cardiac diseases (5) at rest and during training. Monitoring the resting as well as the post-training heart rate (heart rate recovery) is essential because it helps predicting the cardiopulmonary fitness level as well as the mortality risk among evaluated personnel. (6)

Diabetes mellitus is a rapidly growing non-communicable chronic disease worldwide, becoming one of the most alarming health problems in the 21st century. The overall estimated prevalence of diagnosed diabetes in 2018 was 26.9 million US subject of all ages (8.2% of the US population) (7) The International Diabetes Federation (IDF) has estimated the total number of persons with DM across the world will rise from 536.6 million in 2021 to 783.2 million by 2045, with about 94% of the increase in the number of subjects with diabetes by 2045 will be within the low and middle-income countries. The global incidence also projected to increase from 16.3% in 2021 to 19.2% by 2025 in middle- and low-income countries. The prevalence of diabetes in adults (20-79 years old) in the Middle East and North Africa was estimated to be 16.2% compared to 19.3% in 2045. (8) Hypertension possess significantly increased public health risk and population challenge. The prevalence of hypertension was 6.0, 4.2 and 4.9% in male, female and all subjects, respectively. (9) Hypertension prevalence is increasing in KSA, the rate exceeds 25% among the adult Saudi subjects. Monitoring the hypertension-related disturbances is an urgent concept to prevent its organs-damaging. (10) Regional study at Majmaah, Saudi Arabia reported that the hypercholesterolemia prevalence was 45.3%, with no significant difference between both genders. (11) A study by Al-Nozha et al., reported that the hyperlipidemia continues reaching higher prevalence rate recently. The hypercholesterolemia prevalence among the 30-70 years old subjects reached 54.9% and 53.2% for males and females respectively, Hypertriglycemia prevalence was 47.6% in male compared to 33.7% in females. (12) More recently; a study by reported that the prevalence of Hypercholesterolemia among Saudi population ≥ years old is around 12.5%, with males have higher rate (56.7%) compared to females who have lower s rate (43.3%). Close monitoring of the vital signs and cardiovascular variables in patients with chronic non-communicable diseases is indicated since many harmful consequences can be prevented via increasing community awareness and education. (13) Diabetes Mellitus is chronic debilitating disorder requires well-organized efforts and continuous monitoring to limit the impact of disease-associated hazards and long-term complications. (14) The process of SpO2 evaluation is important because it indirectly reflects the subject's organs oxygen requirements. The traditional SpO2 measuring procedure is invasive and painful, requiring collection and assay of arterial blood sample using a blood gas analyzer. (15) Previous trials proposed evaluating the SpO2 non-invasively using simple procedure, with keeping maximum accuracy. (16) Pulse oximetry is a well-known noninvasive instrument used for monitoring and evaluation of SpO2). (17) Routine and frequent screening of patients with chronic diseases is recommended especially with age over 50 years and presence of other comorbidities as HTN and hyperlipidemia. (18) Pulse oximetry is used to measure the level of the SpO2, with low blood flow is associated with lower SpO2. (19) The HR is tightly and linearly correlated with the oxygen consumption at specified time point.(20) Monitoring of other vital variables as the oxygen saturation (SpO2) is recommended in patients suffering hypoxia to improve their survival, (21) as in post-operative and post-arrest cardiac patients, (22) with the pulse oximeter is the widely used instrument to evaluate the SpO2 because of accuracy and ease of application. (23) Quiet recently; the Apple smart watch appeared as a new tool to measure the HR. all the Apple watch versions can monitor the HR, but the blood SpO2 can be only measured by only the latest 6 and 7 versions. The concept of utilizing the Apple watch to measure the HR depends on the Photoplethysmography (PPT) non-invasive measurement procedure applied using wrist-worn watch that continuously monitors both heart beats and blood color changes over time. The PPT is a commonly used approach to measure the cardiac output, blood pressure and SpO2 in verities of medical instruments, (24) that can help discovering the cardiovascular insults and complications at early stages. (25) Implemented new technology and updated features that enable the Apple watch to monitor the HR is available only in updated series-6 and 7. Very limited number of studies evaluated the validity of the Apple watch against pulse oximeter in measuring the SpO2 (the Spo2 was evaluated in 23 patients with chronic obstructive pulmonary disease, 61 patients with interstitial lung diseases and 16 health control subjects). the Apple watch results showed strong positive correlations with that of the pulse oximeter (r=0.81, P<0.0001), furthermore; this study recommended testing the Apple watch validity for measuring the SpO2 in other groups of patients. (26) The Apple watch is a smart instrument with advanced technology measuring the Spo2 and heart rate but its validity in patients with chronic diseases including patients with diabetic mellites, hypertension and hyperlipidemia is still unknown. Therefore, this will be the first study to evaluate the Apple watch accuracy and validity in measuring the Spo2 and heart rate in patients with chronic diseases including diabetic mellitus, hypertension, hyperlipidemia.

Method:

A cross sectional study will be conducted, ninety-five chronic patients will be invited to participate in this study. The study design will be in form of 3-groups: first group will include 35 patients with diabetes and the second group will include 35 patients with hypertension. The third group will be around 35 patients with hyperlipidemia. The distribution of patients and number of groups will be based on the availability of the patients with chronic non-communicable diseases at Umm Al-Qura University Medical Center. All participants in this study will wear the Polar chest strap HR and the Apple Watch at rest, during short session of mild to moderate intensity exercise [50-70% (maximum heart rate-Resting heart rate) + resting heart rate] for 15 minutes and after exercise. The pulse oximeter will be used at rest (pre) and after exercise.

Under resting condition; the pulse oximeter will be fitted on a warm finger while the participant assumes setting position, with the patient in the upright (sitting) position and resting. The SpO2 reading will be recorded after being stabilized on the pulse oximeter instrument. (27, 28) The exercise session will be about 15-minutes duration at mild to moderate intensity according to the heart rate reserve (HRR) using the treadmill and the cycle ergometer, preceded by a 3-minutes warm-up, and followed by 3-minutes cool-down. The HR will be recorded every 30 seconds during whole period and the oxygen saturation will be recorded five times at rest and after exercises.

This study will follow the Declaration of Helsinki 1975 principles, revised in 2000 and will be conducted at the Umm Al-Qura University Medical Center, and will be in line with the Faculty of Applied Medical Sciences, Umm Al-Qura University ethical guidelines. Each participant will sign a written consent approving the volunteer participation in this study and agreeing for publication of its results. Suitable sample size was be computed using the online G-power tool (https://download.cnet.com/G-Power/3000-2054_4-10647044.html), considering the effect size = 0.5, giving a sample size of 54 participants to provide reliable results. Extra-number will be included to substitute any participant's withdrawal or discontinuation.

Inclusion criteria: eligible participants will be patients with chronic diseases as those with stable diabetes mellitus type 1 or 2, hypertension but not more than 180 mm.Hg and patients with hyperlipidemia.

Exclusion criteria: patients with uncontrolled diabetes mellitus, uncontrolled hypertension and hyperlipidemia will be all excluded from the study. Also, patient with other disease rather than that described in the inclusion criteria will be also excluded.

Risk management:

All measurements in this study will be done as the normal measurements for each patient with chronic non-communicable disease who visited the Umm Al-Qura University Medical Center, so there is no risk for the patients to take part in this study. In case any terribly ill happen because of the study procedure, the cardiologist (Dr. Mahmoud) will supervise each patient in this study.

Data analysis:

All data will enter into the SPSS program for analyses. First, a descriptive analysis will be performed to show results in form of means and standard deviations. The results of this study will be analyzed using the Pearson correlation test to test the difference between the apple watch and the Pulse oximeter in measuring SpO2 and heart rate in measuring heart rate to test Apple watch validity. The P value will be set at 0.05 for significant results.

Conditions
Chronic Disease
Being tested
Apple Watch
Keywords
Oxygen saturation, Heart rate, diabetes mellites, Hypertension, hyperlipidemia
Medical subject headings
Chronic Disease, Hypertension, Hyperlipidemias

What participants receive

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

  • Apple WatchDevice

    Apple Watch

Study groups in NCT05271864
Study groupRoleWhat they receive
Group Adiabetes mellites
Receives: Device: Apple Watch
Group Bhypertension
Receives: Device: Apple Watch
Group Chyperlipidemia
Receives: Device: Apple Watch

What is being measured

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

  1. Oxygen Saturation

    Measured: over 10 minutes at rest

  2. Oxygen Saturation

    Measured: over 10 minutes after exercise

Secondary outcomes (1)
  1. Heart rate

    Heart rate

    Measured: over 31 minutes

Timeline

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

  1. First posted9 Mar 2022
  2. Study start1 Nov 2022
  3. Primary completion30 Jul 2023
  4. Study completion30 Jul 2023

Resources

More details

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

Study design
Study type
Observational
Observational model
Other
Time perspective
Cross-sectional
Enrolment
41 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05271864
Sponsor's protocol ID
HAPO-02-K-012-2022-02-959
Status last verified
Nov 2023
First submitted
17 Feb 2022
Last updated
29 Nov 2023
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided: May be for publication in the article

Publications

  • Khushhal AA, Mohamed AA, Elsayed ME. Accuracy of Apple Watch to Measure Cardiovascular Indices in Patients with Chronic Diseases: A Cross Sectional Study. J Multidiscip Healthc. 2024 Mar 11;17:1053-1063. doi: 10.2147/JMDH.S449071. eCollection 2024.

    PubMed 38496326

Questions about this trial

What is this clinical trial studying?

An observational study of Chronic Disease, run by Umm Al-Qura University at 1 site in Saudi Arabia.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 29 Nov 2023. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Saudi Arabia. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Oxygen Saturation (time frame: over 10 minutes at rest). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT05271864, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 29 Nov 2023; AzTrials last refreshed its copy on 7 Nov 2026.

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