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Comparative Effects of Papworth Technique Versus Pranayama in Asthmatic Patients

Not Applicable
Recruiting
Conditions
Asthma
Registration Number
NCT06460597
Lead Sponsor
Riphah International University
Brief Summary

Asthma is a chronic and heterogeneous disease characterized by reversible airway obstruction, airway inflammation and bronchial damage causing dyspnea, wheezing, chest tightness, coughing and impaired quality of life. Papworth technique and Pranayama modify the pattern of breathing to reduce the hyperventilation resulting in normalization of CO2 levels, reduction of bronchospasm and resulting breathlessness

.These techniques also change the emotional stresses, improve the immunity system and improve the strength /endurance of respiratory muscles. After taking the consent form from the participants, data will be collected from Gulab Devi Chest Hospital. Non-Probability Convenience Sampling will be applied on asthmatic patients according to inclusion criteria. Patients will be allocated through simple random sampling into group A and B to collect data. Group A will be treated by Papworth technique. Four weeks will be required to complete the treatment plan. Three sessions will be given for one week so total 12 sessions will be given in one month. Group B will be treated by Pranayama. Four weeks will be required to complete the treatment plan. Three sessions will be given for one week so total 12 sessions will be given in one month. Papworth Technique and Pranayama are used and are assessed to see their effectiveness in asthmatic patients by using four questionnaires on dyspnea, fatigue, anxiety, depression and quality of life. These four standardized questionnaires are Borg Dyspnea Scale (BDS), Modified Fatigue Impact Scale (MFIS), Hospital Anxiety Depression Scale (HADS) and Asthma Quality of life. Pulse oximeter will be used to check the oxygen saturation. The study duration will be completed within time duration of 7 months.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
44
Inclusion Criteria
  • Both genders(male and female)
  • Age 20-40 years
  • Patients with adverse mood effects
  • Mild to moderate chronic asthma
Exclusion Criteria
  • Acute severe asthma
  • Chronic chest infections like TB
  • Chest deformity
  • Bronchiectasis
  • Cardiac Disease
  • Substance abusers
  • Chronic Obstructive Pulmonary Disease
  • Neurological Disorders

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Asthma Quality of lifebaseline and fourth week

It has 32 questions that contains four sub domains, these are symptoms 11 items, activity limitations 12, emotional function 5, environmental stimuli 4 items. This is marked on a 7 point Likert scale that is changing from 1 to 7 where higher scores indicate better quality of life,1 indicates severely impaired patients with asthma while 7 indicates no impairments. Asthma quality of life has strong measurement properties and is valid for measuring health related quality of life in asthma.

Pulse Oximeterbaseline and fourth week

oxygen saturation

Hospital Anxiety Depression Scalebaseline and fourth week

It is a self- assessment scale. It is a reliable instrument for detecting the anxiety and depression in patients with asthma. The anxiety and depressive subscales are also valid measures of severity of emotional stresses. The HADS is a self-report rating scale consists of 14 items on a 4 point Likert Scale range from 0-3.It measures anxiety and depression, 7 items for each subscale. The total score is the sum of 14 items and for each subscale is the sum of respective seven items, ranging from 0-21

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Gulab Devi Chest Hospital Lahore

🇵🇰

Lahore, Punjab, Pakistan

Gulab Devi Chest Hospital Lahore
🇵🇰Lahore, Punjab, Pakistan
Sidra Afzal, PP-DPT
Contact
03124378540
sidra.afzal@riphah.edu.pk
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