The Effect of Precise Aerosol Inhalation Nursing on Sputum Excretion in Elderly Patients With Lung Surgery

Sponsor
The First Affiliated Hospital of Soochow University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05025215
Collaborator
(none)
200
1
2
12
16.7

Study Details

Study Description

Brief Summary

Comparing the effects of different kinds of aerosol inhalation nursing programs on effective sputum excretion in elderly patients with lung surgery.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Precise Aerosol Inhalation Nursing Program
  • Behavioral: Traditional Aerosol Inhalation Nursing Method
N/A

Detailed Description

Based on the traditional oxygen aerosol inhalation treatment, this study will improve it. In the process, precise body position care, time control, observation and treatment, evaluation, etc. will be used to form a precise aerosol inhalation care plan. To explore the effect of this program on effective sputum excretion in elderly patients undergoing lung surgery.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
200 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Study on the Effect of Precise Aerosol Inhalation Nursing Program on Effective Sputum Excretion in Elderly Patients With Lung Surgery
Actual Study Start Date :
May 8, 2021
Anticipated Primary Completion Date :
May 8, 2022
Anticipated Study Completion Date :
May 8, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Group A: Precise

The experimental group accepts improved precise aerosol inhalation nursing program,which was based on the traditional oxygen aerosol inhalation treatment, including precise body position care, time control, observation and treatment, evaluation, etc. This group is planned to enroll 100 patients.

Behavioral: Precise Aerosol Inhalation Nursing Program
The precise aerosol inhalation nursing program was based on the traditional oxygen aerosol inhalation treatment, including precise body position care, time control, observation and treatment, evaluation, etc.

Experimental: Group B:Traditional

The control group accepts traditional aerosol inhalation nursing method. This group is planned to enroll 100 patients.

Behavioral: Traditional Aerosol Inhalation Nursing Method
The traditional aerosol inhalation nursing method is carried out according to the operation of aerosol inhalation.

Outcome Measures

Primary Outcome Measures

  1. Standardization of aerosol inhalation [From the first to the third day after surgery.]

    The investigators use a self-made inhalation implementation standard evaluation form to evaluate whether inhalation was standard in postoperative patients.

Secondary Outcome Measures

  1. Adverse events [From the first to the third day after surgery.]

    Discomfort during inhalation: chest tightness, dyspnea, palpitations, elevated blood pressure, etc.

  2. Viscosity of sputum [From the first to the third day after surgery.]

    According to the viscosity, the sputum was divided into three types: ⅰ degree (thin phlegm), ⅱ degree (moderate phlegm), ⅲ degree (severe phlegm).

  3. Phlegm retention [From the first to the third day after surgery.]

    Sputum sounds can be heard or ausculted at the bedside.

  4. Patient satisfaction [The third day after surgery.]

    Likert 5-level scoring method was adopted to allow patients to evaluate the nursing plan. The higher the score, the more satisfied the patients were.

Eligibility Criteria

Criteria

Ages Eligible for Study:
65 Years to 79 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • ①The patient underwent thoracoscopic lung surgery; ②There was no obvious pulmonary infection before the operation; ③Good audiovisual function, no communication barriers, able to cooperate with nebulized inhalation operation; ④Patients informed consent to this study.
Exclusion Criteria:
  • ①Patients with mental illness; ②Acute COPD; ③Serious complications or failure of important organs after operation.

Contacts and Locations

Locations

Site City State Country Postal Code
1 The First Affiliated Hospital of Soochow University Suzhou China

Sponsors and Collaborators

  • The First Affiliated Hospital of Soochow University

Investigators

  • Principal Investigator: Jing Luo, The First Affiliated Hospital of Soochow University

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
The First Affiliated Hospital of Soochow University
ClinicalTrials.gov Identifier:
NCT05025215
Other Study ID Numbers:
  • 20210822
First Posted:
Aug 27, 2021
Last Update Posted:
Aug 27, 2021
Last Verified:
Aug 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 27, 2021