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Positive effect of yoga practice and natural therapy (naturopathy) on asthma (breathing problem) in children.

EFFICACY OF YOGA AND NATUROPATHY PROTOCOL ON SELECTED PSYCHOLOGICAL AND PHYSIOLOGICAL FACTORS IN ASTHMATIC CHILDREN - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/12/098857
Enrollment
60
Registered
2025-12-10
Start date
Unknown
Completion date
Unknown
Last updated
2026-01-12

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

Conditions

Health Condition 1: J459- Other and unspecified asthma

Interventions

Intervention1: YOGA PRACTICES: 1. Bhujangasana 2. Setu Bandhasana 3. Matsyasana 4. Sessional Breathing 5. AnulomVilom 6. Bhramari Pranayama Intervention2: YOGA PRACTICES AND NATUROPATHY PROTOCOL: 1. B

Sponsors

Satyaki Chakraborty
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Age: Participants must be 8-15 years old. 2. Residence: Currently residing at West Bengal. 3. Genders: Children will be of both genders 4. Cognitive status: Able to follow simple instructions and provide informed consent. 5. Language: Able to communicate in Bengali / English / Hindi to understand instructions and provide feedback. 6. Willingness: Agree to participate procedures.

Exclusion criteria

Exclusion criteria: 1. Children with chronic cardiac, chronic pulmonary disease and immunodeficiency. 2. Children with gross motor/central nervous system (CNS) deficit disabled to perform yoga exercises. 3. Children with chronic sinusitis, chronic chest conditions including infection, congenital heart diseases, Musculo-skeletal deformities, neuro-muscular disorders. 4. any other chronic conditions.

Design outcomes

Primary

MeasureTime frame
Primary outcomes are- 1.Increment in mean Peak Expiratory Flow Rate (PEFR). 2.Increment in mean Childhood Asthma Control Test (C-ACT) scores. 3.Increment in mean Pediatric Asthma Quality of Life Questionnaire (PAQLQ) scores. 4.Changes in Absolute Eosinophil Count (AEC). 5.Changes in C-Reactive Protein (CRP) values. 6.Changes in Immuno-Globulin E (IgE) values. 7.Changes in Serum Cortisol levels. Timepoint: Duration- 3 months. Pre-test will be conducted for all the experimental groups at the beginning of the study (Baseline). Post-test will be conducted for all the experimental groups after 3 months of intervention (except control group).—

Secondary

MeasureTime frame
NOT APPLICABLETimepoint: NOT APPLICABLE—

Countries

India

Contacts

Public ContactSATYAKI CHAKRABORTY

Manipur University

ghosh.kun@gmail.com9986847269

Outcome results

None listed

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