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Feasibility of Implementing a non-invasive Self Sampling method of saliva specimen for the diagnosis of respiratory infections respiratory infections

Feasibility of Implementing a non-invasive Self Sampling method of saliva specimen that can be used for the diagnosis of respiratory infections among population groups in Tshwane district

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
PACTR
Registry ID
PACTR202411743094783
Enrollment
100
Registered
2024-11-04
Start date
2024-11-11
Completion date
Unknown
Last updated
2026-09-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Respiratory

Interventions

Candycollect lollipop

Sponsors

None listed

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: • Various populations in the underserved communities within the Tshwane District who agree to participate In the study such as community members, healthcare workers within that community and researchers whose research focus is diagnosing of respiratory pathogens and infections • Children between the ages of 3-112 years old • Adults of all ages who are willing to participate

Exclusion criteria

Exclusion criteria: • Various populations in the underserved communities within the Tshwane district not willing to participate in the study • Participants in the underserved communities within the Tshwane district who decide to not complete the study • Population groups not within the underserved communities of the Tshwane district.

Design outcomes

Primary

MeasureTime frame
User satisfaction: Satisfaction with the self-sampling method: Assess users' satisfaction levels with the non-invasive self-sampling process, including ease of use, convenience, and comfort. Satisfaction with the POC diagnostic technologies: Evaluate users' satisfaction with the digital-linked molecular-based POC diagnostic devices, considering factors such as user-friendliness, clarity of instructions, and overall experience. ;Acceptability: Willingness to use the self-sampling method: Determine users' willingness to adopt and utilize the non-invasive self-sampling method as part of their regular healthcare routine. Perception of convenience: Assess users' perception of the convenience and accessibility of the self-sampling method compared to traditional invasive sampling methods.

Secondary

MeasureTime frame
User preferences and barriers: User preferences: Identify user preferences regarding the frequency of self-sampling, ease of sample collection, and preferences for digital-linked POC diagnostic technologies. Barriers to adoption: Explore any potential barriers or concerns expressed by users that may hinder the widespread adoption of the non-invasive self-sampling method and POC diagnostic technologies.

Countries

South Africa

Contacts

Public ContactGertrude Mamabolo

Senior Management Assistant

gertrude.mamabolo@up.ac.za0123192198

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Sep 19, 2026