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TuberculosisCaPThaiNCT05581212

TB Case-Finding, Treatment and Prevention Intervention in Thailand

A study testing Tuberculosis Case-Finding, Treatment and Prevention Public Health Pack in people with Tuberculosis, run by Institut de Recherche pour le Developpement at 20 sites in Thailand.

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

The project aimed to test a strategy for the early detection and prevention of tuberculosis in household contacts of tuberculosis patients in order to reduce the morbidity, mortality and transmission of this disease in Thailand. Read more about this study

Who is it for?
Any ageHealthy volunteers can take part
Conditions the study is for
Tuberculosis
What is being tested?
Tuberculosis Case-Finding, Treatment and Prevention Public Health Pack
Could I receive a placebo?
No, everyone receives an active treatment
How many people
7,455 participants
Where
20 sitesThailand
Study dates
7 May 2024to 7 Jan 2026
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 Any age
  • All sexes
  • Healthy volunteers accepted
  • Child, Adult, Older adult

Who may be able to join

  • Age ≥18 years
  • Newly bacteriologically confirmed TB case (within 1 month of diagnosis)
  • Living in the same household for the last 3 months
  • Reporting at least one HH contact
  • Providing written informed consent for participation in the study
  • All contacts living in the same HH, defined as any person who shared the same enclosed living space as the index TB case for one or more nights or for frequent or extended daytime periods for at least one month before the TB diagnosis is made.
  • Providing written informed consent (signed by adult (≥18 years) contacts; or by parents/guardians for minors < 13 years or incapacitated people; written assent for children ≥13 years and < 18 years).

Who cannot join

  • Index case who do not live in the catchment area of the study cluster
  • Index cases diagnosed with rifampicin resistance, multidrug resistance (MDR) or extensively drug-resistant (XDR-TB)
  • Index cases who are incarcerated
  • contact currently on TPT or on TB treatment or who finished such treatment in the last 3 months.

Trial locations and contacts

20 sites in 1 country.

20 sites in 1 country

Thailand20 sites
  • Bang Lamung H.

    Bang Lamung

  • Nakornping H.

    Chiang Mai

  • Chiangrai Prachanukroh H.

    Chiang Rai

  • Chon Buri H.

    Chon Buri

  • Kalasin H.

    Kalasin

  • Khon Kaen H.

    Khon Kaen

  • Lampang H.

    Lampang

  • Samut Prakan H.

    Mueang Samut Prakan

  • Buriram H.

    Nakhon Ratchasima

  • Surin H.

    Nakhon Ratchasima

  • Maharaj Nakhon Si Thammarat H.

    Nakhon Si Thammarat

  • Phra Nakhon Si Ayutthaya H.

    Phra Nakhon Si Ayutthaya

  • Ratchaburi H.

    Ratchaburi

  • Samut Sakhon H.

    Samut Sakhon

  • Si Sa Ket H.

    Si Sa Ket

  • Hat Yai H.

    Songkhla

  • Songkhla H.

    Songkhla

  • Surat Thani H.

    Surat Thani

  • Trang H.

    Trang

  • Sunpasitthiprasong H.

    Ubon Ratchathani

Other trials in Thailand

About this study

Official title: Implementation of a New Strategic TB Case-Finding, Treatment and Prevention Public Health Pack in Thailand

The project aimed to test a strategy for the early detection and prevention of tuberculosis in household contacts of tuberculosis patients in order to reduce the morbidity, mortality and transmission of this disease in Thailand. This strategy will be evaluated in comparison with the current programmatic approach through a pragmatic trial with cluster randomization (cluster randomized controlled trial) which will be conducted over the next 3 years. This project is carried out in collaboration with the Tuberculosis Division of the Ministry of Public Health of Thailand, the TB/HIV Research Foundation in Thailand and the London School of Hygiene and Tropical Medicine in England.

Read the detailed description

Title: Implementation of a new Strategic TB Case-Finding, Treatment and Prevention Public Health Pack in Thailand (CapThai) Phase: IV, cluster randomized trial

Population:

adults (>= 18 years old) with pulmonary TB and their household contacts. Sites: 20 clusters (provincial hospitals) in Thailand

Duration of the study:

36 months

Subject participation duration:

9 months

Description of the intervention:

Combined active case-finding, treatment and prevention of TB amongst household contacts of TB cases, associated with initiation of SOC treatment in active TB cases and initiation of TB preventive therapy in those contacts without active TB, based on free screening. This intervention will be compared to the standard of care available in the country.

Overall objective:

To evaluate whether a public health intervention package focusing on the households of newly detected TB cases can increase active case-finding and uptake of TB preventive therapy in Thailand.

Specific objectives:

  1. to compare the initiation and completion of TPT regimens amongst household contacts of infectious TB patients, overall and by gender and age group;
  2. to evaluate the safety of short TPT regimens amongst HH contacts, overall and by gender and age group;
  3. to compare the detection of TB and treatment uptake for active TB amongst HH contacts of infectious TB patients, overall and by gender and age group;
  4. to assess the feasibility of the combined intervention among health care providers and beneficiaries, by gender and age group;
  5. to assess the acceptability of the combined intervention among health care providers and beneficiaries, by gender and age group;
  6. to evaluate the epidemiological impact of the combined intervention.

Study design:

The study uses a Stepped-Wedge Cluster Randomised Trial design. Randomisation will take place at the hospital level (cluster: provincial hospitals with >150 new TB cases/year). Twenty clusters will be enrolled and switch from the control to the intervention phase in four sequences every 3 months in a random order until all clusters are exposed to the intervention.

  1. Intervention Phase: Newly detected bacteriologically confirmed TB patients (≥ 18 years) will be sensitized on the importance of HH contact investigation and TB stigma reduction. They will be asked to enumerate all contacts (name/age/sex/relationship) living in their HH for>1 month at the date of TB diagnostic. Screening invitation cards will be provided for each HH contact (or caregiver for children <13 years old), inviting them to attend the TB clinic at the selected hospital for free screening and evaluation. Transportation fees will be provided. Contacts detected with active TB will receive recommended treatment. In contacts for whom active TB is formally excluded, TPT will be initiated with the new short regimens: (i) children <2 years: isonicotine hydrazine (INH)+rifampicin daily for 3 months; (ii) children 2-12 years: INH+rifapentine weekly for 3 months; (iii) children≥13 and adults: INH+rifapentine daily for 1 month.
  2. Control phase: current strategy relying on passive case detection and advice provided to TB patients to refer HH contacts to the TB clinic for screening. The index TB patient will be asked to enumerate HH contacts as above and inform them on the need to be screened at the TB clinic.

Endpoints:

Primary endpoint: Proportion of HH contacts with active TB excluded who are initiated on TPT within 4 weeks of the index TB patient diagnosis - overall, by age group (<15, ≥15 years) and gender.

Secondary endpoints:

  1. Proportion of participants initiated on TPT who completed TPT;
  2. Proportion of participants in the Intervention phase who were initiated on TPT for whom treatment is discontinued due to intolerance, adverse events, or severe adverse events;
  3. Proportion of HH contacts with newly diagnosed active TB initiated on curative treatment within 8 weeks of the index TB case diagnosis - overall, by age group (<15, ≥15 years) and gender;
  4. Proportion of household contacts diagnosed with TB who completed TB treatment in the intervention vs. control phase;
  5. Proportion of contacts receiving TPT who developed TB over the 9 months follow-up period in the intervention vs. control phase.

Estimated time to complete enrollment:

12-15 months

Conditions
Tuberculosis
Being tested
Tuberculosis Case-Finding, Treatment and Prevention Public Health Pack
Keywords
Case-finding, Preventive treatment, Public Health Pack, Household contacts
Medical subject headings
Tuberculosis

What participants receive

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

  • Tuberculosis Case-Finding, Treatment and Prevention Public Health PackOther

    Combined active case-finding, treatment and prevention of TB amongst HH contacts of TB cases, associated with initiation of standard of care (SOC) treatment in active TB cases and initiation of TB preventive therapy in those contacts without active TB, based on free screening. This intervention will be compared to the standard of care available in the country.

Study groups in NCT05581212
Study groupRoleWhat they receive
Standard of Care (Control phase)No interventionIn the current standard of care in Thailand, at time of diagnosis and tuberculosis (TB) treatment initiation, TB patients are being advised to tell their household (HH) contacts to consult at the TB clinic for screening and provision of either curative or preventive treatment - according to the screening outcome.
Tuberculosis Case-Finding, Treatment and Prevention Public Health Pack (Intervention phase)ExperimentalIn the selected provinces, individuals (≥18 years) with newly detected bacteriologically confirmed pulmonary Tuberculosis (index TB case) will be sensitized on the importance of HH contact investigation for detection and prevention of TB and stigma reduction. Index TB cases will be asked to enumerate all persons living in their HH for ≥1 month at the date of TB diagnostic (contact list), and provide their name/age/sex and relationship with the index case. Screening will be offered to each HH contact, using screening invitation cards that will be provided to the index TB case, to be handed over to each HH contact (or caregiver for children <13 years old). Urban and Village Health Volunteers (U/VHV),will visit the HH to enhance awareness of the importance of screening for TB case-finding and prevention and facilitate liaison with the hospital. If active tuberculosis has been formally excluded, they will be eligible to receive the Tuberculosis Preventive Treatment (TPT).
Receives: Other: Tuberculosis Case-Finding, Treatment and Prevention Public Health Pack

What is being measured

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

  1. Proportion of household contacts with active tuberculosis excluded who are initiated on tuberculosis preventive treatment within 4 weeks of the index tuberculosis patient diagnosis - overall

    Proportion of household contacts with active tuberculosis excluded who are initiated on tuberculosis preventive treatment within 4 weeks of the index tuberculosis patient diagnosis - overall

    Measured: Month18

  2. Proportion of household contacts with active tuberculosis excluded who are initiated on tuberculosis preventive treatment within 4 weeks of the index tuberculosis patient diagnosis - by age group (<15, ≥15 years)

    Proportion of household contacts with active tuberculosis excluded who are initiated on tuberculosis preventive treatment within 4 weeks of the index tuberculosis patient diagnosis - by age group (<15, ≥15 years)

    Measured: Month18

  3. Proportion of household contacts with active tuberculosis excluded who are initiated on tuberculosis preventive treatment within 4 weeks of the index tuberculosis patient diagnosis - by gender

    Proportion of household contacts with active tuberculosis excluded who are initiated on tuberculosis preventive treatment within 4 weeks of the index tuberculosis patient diagnosis - by gender

    Measured: Month18

Secondary outcomes (5)
  1. Proportion of participants initiated on TPT who completed TPT

    Proportion of participants initiated on TPT who completed TPT

    Measured: Month 18

  2. Proportion of participants who initiate TPT for whom treatment is discontinued due to adverse events or intolerance in the Intervention phase

    Proportion of participants who initiate TPT for whom treatment is discontinued due to adverse events or intolerance in the Intervention phase

    Measured: Month 18

  3. Proportion of HH contacts with newly diagnosed active TB initiated on curative treatment within 4 weeks of the index TB patient diagnosis - overall

    Proportion of HH contacts with newly diagnosed active TB initiated on curative treatment within 4 weeks of the index TB patient diagnosis - overall

    Measured: Month 18

  4. Proportion of HH contacts with newly diagnosed active TB initiated on curative treatment within 4 weeks of the index TB patient diagnosis - by age group (<15, ≥15 years)

    Proportion of HH contacts with newly diagnosed active TB initiated on curative treatment within 4 weeks of the index TB patient diagnosis - by age group (<15, ≥15 years)

    Measured: Month 18

  5. Proportion of HH contacts with newly diagnosed active TB initiated on curative treatment within 4 weeks of the index TB patient diagnosis - by gender

    Proportion of HH contacts with newly diagnosed active TB initiated on curative treatment within 4 weeks of the index TB patient diagnosis - by gender

    Measured: Month 18

Timeline

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

  1. First posted14 Oct 2022
  2. Study start7 May 2024
  3. Primary completion6 Jan 2026
  4. Study completion7 Jan 2026

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
Sequential
Model description
Stepped-Wedge Cluster Randomised Trial design
Masking
None (open label)
Enrolment
7,455 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05581212
Sponsor's protocol ID
IRD-1-001
Other IDs
21SANIN207
Acronym
CaPThai
Status last verified
Apr 2026
First submitted
17 Jun 2022
Last updated
29 Apr 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No

Publications

  • Tovar Sanchez T, Ngamvithayapong-Yanai J, Grint D, Beneteau S, Luangjna S, Ouedraogo S, Lachenal N, Bonnet M, Fielding K, Kamolwat P, Lienhardt C. Evaluation of a combined tuberculosis case-finding, treatment and prevention strategy in Thailand: protocol for a pragmatic phase IV stepped-wedge cluster-randomised trial, the CaPThai study. Trials. 2026 Feb 16;27(1):225. doi: 10.1186/s13063-026-09532-7.

    PubMed 41699679

Questions about this trial

What is this clinical trial studying?

A study testing Tuberculosis Case-Finding, Treatment and Prevention Public Health Pack in people with Tuberculosis, run by Institut de Recherche pour le Developpement at 20 sites in Thailand.

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 7 inclusion and 4 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 Apr 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 20 sites in Thailand. 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?

Proportion of household contacts with active tuberculosis excluded who are initiated on tuberculosis preventive treatment within 4 weeks of the index tuberculosis patient diagnosis - overall (time frame: Month18). The study lists 3 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 NCT05581212, 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 Apr 2026.

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