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Clinical Trials/NCT05936801
NCT05936801CompletedNot Applicable

Comparative Effects of Anterior Chest Compression Assist and Abdominal Thrust Assist Technique on Sputum Diary, Oxygen Saturation, Expiratory Flow Rate, and Dyspnea in Patients With Chronic Obstructive Pulmonary Disease

Riphah International University1 site in 1 country34 target enrollmentStarted: July 15, 2023Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
34
Locations
1
Primary Endpoint
Oxygen saturation

Study Overview

Brief Summary

A total 34 patients will be taken. 2 groups will be created to apply intervention. After signing consent form, 17 patients in group A will be given abdominal thrust assist technique and 17 patients in group B will be given anterior chest compression technique.

Detailed Description

Patient is instructed to take in a deep breath and hold it. Then, just as the patient is instructed to cough, the therapist applies a quick push up and in under the diaphragm with the heel of the hand. In Anterior chest compression: the therapist places one arm across the patient's pectorals and the other parallel to it. After the patient takes a maximal breath, the therapist pushes down to help the patient cough. The greatest force is applied through the lower chest during expulsion. A total 34 patients will be taken. 2 groups will be created to apply intervention. After signing consent form, 17 patients in group A will be given abdominal thrust assist technique and 17 patients in group B will be given anterior chest compression technique. Baseline treatment given to both groups will include percussion and tapping. The data collected will then be analyzed using IBM SPSS version 25.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Participant)

Masking Description

A total 34 patients will be taken. 2 groups will be created to apply intervention. After signing consent form, 17 patients in group A will be given abdominal thrust assist technique and 17 patients in group B will be given anterior chest compression technique. Baseline treatment given to both groups will include percussion and tapping. The data collected will then be analyzed using IBM SPSS version 25

Eligibility Criteria

Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •uncontrolled Tachycardia
  • •Unconscious patients
  • •In neuro-compromised patients with Cognitive dysfunction
  • •Recent esophageal surgery
  • •Acute abdominal distension -Recent Broncho-pleural fistula - Pulmonary embolism, pneumothorax hemothorax
  • •Unstable head and neck fracture

Exclusion Criteria

  • •Breathlessness, Cough and sputum scale (BCSS)
  • •Modified Borg Dyspnea scale
  • •Peak Flow Meter
  • •Pulse Oximeter

Arms & Interventions

Anterior Chest Compression technique

Experimental

Baseline treatment given is percussion and vibration in side lying position. The therapist puts one arm across the patient's pectoral region to stabilize or compress the upper chest while the other arm is placed either parallel on the lower chest or abdomen below the xiphoid process. Inspiration is facilitated by the pressure on anterior chest, followed by a "hold."

Just as the patient is instructed to cough, the therapist applies a quick force with both arms:

down and back on the upper chest and up and back on the lower chest or abdomen. 3 sessions in a wk would be given on alternate days

Intervention: Anterior Chest Compression technique (Other)

Abdominal Thrust Technique

Experimental

Baseline treatment given is percussion and vibration in side lying position. It Can be used in both the supine and side lying positions. With the patient in the supine position, the therapist places the heel of one hand inferior to the patient's xiphoid process and below the patient's lower ribs.

Intervention: Abdominal Thrust Technique (Other)

Outcomes

Primary Outcomes

Oxygen saturation

Time Frame: 4 weeks

oxygen saturation will be measure with pulse oximeter.

sputum diary

Time Frame: 4 weeks

sputum of each patient will be recorded.

expiratory flow rate

Time Frame: 4 weeks

Expiratory flow rate will be measured through peak expiratory flow meter

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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