Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2026-03-26 @ 3:18 PM
Ignite Modification Date:
2026-03-26 @ 3:18 PM
NCT ID:
NCT07432893
Eligibility Criteria:
Inclusion Criteria:
1. Adults aged ≥18 years
2. Presenting to participating primary care facilities in study sites
3. Meeting criteria for at least one of the following conditions or symptoms:
* Hypertension: Known diagnosis
* Diabetes mellitus: Known diagnosis or laboratory evidence (HbA1c ≥6.5%, fasting blood glucose ≥126 mg/dL, or post-prandial glucose ≥200 mg/dL)
* Fever: Presenting as chief complaint
* Breathlessness: Presenting as chief complaint, without evidence of fever
* Musculoskeletal pain: Presenting as chief complaint, without evidence of fever
4. Able and willing to provide written informed consent
5. Willing to participate in two sequential consultations and complete an exit survey
Exclusion Criteria:
1. Inability to provide informed consent due to cognitive impairment (e.g., dementia or intellectual disability)
2. Medical instability or condition requiring immediate emergency referral
3. Prior participation in the study during an earlier visit
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT07432893
Study Brief:
Protocol Section:
NCT07432893