Actively Recruiting

Phase Not Applicable
Age: 6Years - 17Years
All Genders
NCT07097961

Paediatric Post-TB Pulmonary Rehab Study

Led by University of Iowa · Updated on 2025-08-11

40

Participants Needed

1

Research Sites

29 weeks

Total Duration

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Sponsors

U

University of Iowa

Lead Sponsor

M

MU-JHU CARE

Collaborating Sponsor

AI-Summary

What this Trial Is About

The goal of this clinical trial is to learn if a home-based pulmonary rehabilitation program is feasible and acceptable for children ages 6-15 who have recently completed treatment for pulmonary tuberculosis. The main questions it aims to answer are: Can children and caregivers follow a 6-week rehabilitation program? Is the program acceptable and feasible for children and caregivers? Researchers will also explore preliminary changes in walking distance and quality of life. Participants will: Attend a clinic visit for baseline testing, including a 6-minute walk test (6MWT) and the St. George's Respiratory Questionnaire (SGRQ) Receive exercise instructions and a pedometer Complete home-based walking and wall sit exercises twice per week for 6 weeks Receive weekly follow-up from study staff (by phone or home visit) Return to clinic at 6 weeks for follow-up testing

CONDITIONS

Official Title

Paediatric Post-TB Pulmonary Rehab Study

Who Can Participate

Age: 6Years - 17Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Aged 6-17 years
  • Previously diagnosed with post-TB lung disease
  • Willing to remain in the study catchment area during the study period
  • Able to participate in mild-to-moderate physical activity
Not Eligible

You will not qualify if you...

  • Currently participating in another rehabilitation program
  • Residence outside the Kampala metropolitan area
  • Active respiratory infection

AI-Screening

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Trial Site Locations

Total: 1 location

1

MU-JHU Care Ltd/MU-JHU Research Collaboration

Kampala, Uganda

Actively Recruiting

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Research Team

G

Greta L Becker, MD

CONTACT

B

Brooks Jackson, MD, MBA

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

OTHER

Number of Arms

1

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