Designing, Development and testing of RK RespoTech Respiration Enhancing Device

Validation and Testing of RK RespoTech Respiration Enhancing Device

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2022/04/042298

Enrollment

105

Registered

2022-04-29

Start date

Unknown

Completion date

Unknown

Last updated

2022-05-02

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

Conditions

Health Condition 1: J988- Other specified respiratory disorders

Interventions

Intervention1: hand held portable device with Mobile Application for Physiotherapy assessment and Treatment: Self developed hand held device with mobile application for screening of Respiratory Disord

Eligibility

Inclusion criteria

Inclusion criteria: patients with respiratory disorders

Exclusion criteria

Exclusion criteria: Subjects those who have smoking history Subjects who are not able to blow Long term coughing history Recent eye surgery and head injury Those who have difficulty in opening and closing of mouth

Design outcomes

Primary

Measure	Time frame
FEV1 (FORCED EXPIRATORY VOLUME IN ONE SECOND) PEFR (PEAK EXPIRATORY FLOW RATE) Timepoint: ONE TIME	—

Secondary

Measure	Time frame
PCO2 in expirationTimepoint: one time	—

Countries

India

Contacts

Public ContactVIDHI JOSHI

School of Physiotherapy, Physiotherapy Department, RK University

priyanshu.rathod@rku.ac.in9426803108

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026