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AzTrials

COVID-19NCT05614388

A Study on Voluntary Routine COVID-19 Self-testing in Mizoram, India.

A study testing COVID-19 Self testing and related messaging in people with COVID-19, run by PATH.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

This interventional study aims to evaluate the utilization, adherence, and acceptability of voluntary, free, routine self-testing for COVID-19 (Corona Virus (19) Disease) and related information, education and communication (IEC) messages in two institutional settings in Mizoram, India. Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
Conditions the study is for
COVID-19
What is being tested?
COVID-19 Self testing and related messaging
Could I receive a placebo?
No, everyone receives an active treatment
How many people
646 participants
Where
No sites listed yet
Study dates
Dec 2022to May 2023
Phase
Interventional
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 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • Above the age of 18 years, irrespective of gender and past COVID-19 status
  • Registered with participating institutions
  • Able and willing to provide informed consent
  • Owns a smartphone capable of downloading the SURE STATUS app for uploading results
  • Able to read the instructions in the Mizo or English or Hindi

Who cannot join

  • Does not consent.
  • Has any contraindication to nasal sample collection, including recent nasal injury, nasal surgeries.
  • Personnel who are directly involved in the conduct of the study, e.g., investigator, sub-investigator, research assistant, pharmacist, study coordinator or anyone mentioned in the delegation log.

Trial locations and contacts

No sites are listed yet.

Muneer Kutty, MPH contact

+919999798283

mkutty@path.org

About this study

Official title: A Study on Utilization, Adherence, and Acceptability of Voluntary Routine COVID-19 Self-testing Among Students, Staff and Health Workers at Two Institutions in Mizoram, India.

This interventional study aims to evaluate the utilization, adherence, and acceptability of voluntary, free, routine self-testing for COVID-19 (Corona Virus (19) Disease) and related information, education and communication (IEC) messages in two institutional settings in Mizoram, India. In addition, it will assess and measure preferences for assisted vs unassisted and observed vs unobserved self-testing, assess adherence and measure dropout rate and describe dropout characteristics.

The research questions it aims to address are -

  1. What is the uptake and adherence of voluntary, free, routine self-testing for COVID-19 and related IEC messages vy students, employees, and healthcare workers in two institutional settings in India? Are there any dropouts from routine self-testing and what are the factors related to dropouts?
  2. What is the preferred mode of self-testing- observed or unobserved, assisted or unassisted? Do these preferences change over time? The researchers will be measuring - Utilization rate, Adherence rate, Proportion of preference to assisted vs unassisted self-testing, Proportion of preference to observed vs unobserved self-testing, Time to dropout and Acceptability of COVID-19 self-testing kits.
Read the detailed description

Testing is a critical component of the pandemic response. It serves two purposes; for clinical purposes, it focuses on identifying disease in symptomatic patients, while testing for epidemiological purposes, spread in the population is also assessed. India uses a mix of both Reverse Transcriptase Polymerase Chain Reaction (RT PCR) and Antigen Rapid Diagnostic Tests (Ag RDTs) for COVID-19 testing. RT PCR is the reference standard test for detection of the virus. However, not all facilities have RT PCR, and many communities have poor access. This leads to a long turn-around time (TAT) for the results to be obtained and a high load on RT PCR facilities. Hence, to prevent the spread of the virus, cases must get detected early. At the peak of the first wave of the pandemic in the country, Ag RDTs constituted close to 50% of all the tests conducted in the country. Self-testing for COVID-19 has emerged as a viable complementary testing modality. The use of self-testing kits while ensuring the availability of other COVID-19 tests at the nearest point of care addresses many of the usual barriers to uptake of services, leading to timely testing of individuals, diagnosis, and access to care. It can also reduce the burden on existing testing infrastructure especially during a surge in the cases. It also reduces overcrowding at testing facilities thereby reducing the risk of disease transmission. To improve access to testing and prevent overreliance on RT PCR laboratories, the Indian Council of Medical Research (ICMR) approved and validated the use of COVID-19 self-testing kits. As of March 2022, sixteen self-testing kits have been validated in India of which 10 are found to be satisfactory. While there are many benefits to self-testing, it is also essential to understand the utilization of the self-testing strategy, including whether or not the community can follow the steps for self-testing and what support, if any, the community may require to use self-test kits.

The present study proposes the demonstration of ICMR and US-FDA (United States Food \& Drug Administration) approved SURE STATUS self-testing kit in the healthcare workers and educational institution setting in Mizoram for a period of 5 months. With the ease of lockdown and movement restrictions, workplaces and educational institutes are gradually opening up. However, with the threat of the pandemic still looming large, it is prudent to put in place systems for regular screening within these settings to promote early diagnosis and care and prevent outbreaks. COVID-19 self-test has been identified as one way any institution can scale up COVID-19 testing to improve COVID-19 status awareness by reaching out to as many people as possible at a given point of time.

While COVID-19 self-tests are available and widely used in India, these kits are largely used within the confines of individual homes. It is learnt that the reporting of the results of the self-test is poor as compared to the utilization of the self-test kits. To the investigator's knowledge, no study has been conducted in India to assess the utilization of self-testing as a routine procedure in places of mass indoor gathering, like workplaces and educational institutions. To address this gap, the investigators will conduct a study to evaluate the utilization, adherence, and acceptability of routine COVID-19 self-testing among students, employees and healthcare workers in two congregate settings: one University College and one Medical College and Hospital in Mizoram, India. The proposed study will document challenges, if any, in reporting of self-test results and document the key processes in operationalizing routine COVID-19 self-testing among students, employees and healthcare workers and provide learning and recommendations for systematic use of self-tests for future models of institution based COVID-19 self-testing in congregate settings.

Conditions
COVID-19
Being tested
COVID-19 Self testing and related messaging
Keywords
COVID 19, Self-Test, Pandemic Preparedness, Infectious diseases
Medical subject headings
COVID-19, Communicable Diseases

What participants receive

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

  • COVID-19 Self testing and related messagingDiagnostic test

    Provisioning of voluntary, free self-testing for COVID-19 (approved and validated in the country) and related Information, Education and Communication (IEC) messages

Study groups in NCT05614388
Study groupRoleWhat they receive
Study participantsExperimentalThe study procedure is universal to all the participants from both the institutes. There are no control arms defined separately. The groups within the participants include - include health care workers, non-medical hospital staff and medical students at ZMC; and faculty, students and supporting staff at the Pacchunga University College.
Receives: Diagnostic Test: COVID-19 Self testing and related messaging

What is being measured

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

  1. Utilization rate

    Individual level: the proportion of tests each individual uses till the end of the follow-up period from the minimum number of tests allocated to them.

    Sample-level: mean and standard deviations calculated based on the individual utilisation rates

    Measured: 5 Months

  2. Adherence Rate

    Individual level: the proportion of tests an individual performs according to the testing schedule over the total number of tests they perform.

    Sample-level: mean and standard deviations calculated based on the individual adherence rates

    Measured: 5 Months

  3. Preferences of participants on self testing

    Proportion of preference to assisted vs unassisted self-testing

    Measured: 5 Months

  4. Observation proportions of participants on self testing

    Proportion of preference to observed vs unobserved self-testing

    Measured: 5 Months

  5. Time to dropout

    The time to drop out will be the time from enrolment of the participant till drop-out

    Measured: 5 Months

  6. Acceptability of COVID-19 self-testing kits

    A composite indicator based on ease of use of COVID-19 self-testing kits, ease of interpretation of test results, and recommendation to others

    Measured: 5 Months

Timeline

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

  1. First posted14 Nov 2022
  2. Study startDec 2022 (estimated)
  3. Primary completionApr 2023 (estimated)
  4. Study completionMay 2023 (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
Diagnosis
Allocation
Not applicable
Intervention model
Single group
Model description
The participants include health care workers, non-medical hospital staff and medical students at ZMC; and faculty, students and supporting staff at the Pacchunga University College. All these groups will be participating in the study simultaneously. The study results will be compared for all these 6 groups.
Masking
None (open label)
Enrolment
646 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05614388
Sponsor's protocol ID
RES-376
Status last verified
Nov 2022
First submitted
9 Nov 2022
Last updated
21 Nov 2022
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: We do not plan to share any individual participant data. We will share collective learnings on various parameters at both the sites.

Questions about this trial

What is this clinical trial studying?

A study testing COVID-19 Self testing and related messaging in people with COVID-19, run by PATH.

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 5 inclusion and 3 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: status not confirmed, as of the sponsor's last update on 21 Nov 2022. Status can change between updates, so confirm with the study contact before making plans.

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?

Results are not available in the source record.

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

Contact Muneer Kutty, MPH (+919999798283, mkutty@path.org), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Utilization rate (time frame: 5 Months). The study lists 6 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
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 21 Nov 2022.

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Clinical Trial NCT05614388 | AzTrials