Effect of SMS Use on Postoperative Respiratory and Cough Exercise Compliance

Surgery Clinical Trial

Official title:

Effect of SMS Reminder Use on Postoperative Respiratory and Cough Exercise Compliance of Patients After Lung Cancer Surgery

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05915221
• Other study ID #: 2021/526
• Status: Completed
• Phase: N/A
• Start date: February 1, 2022
• Est. completion date: April 3, 2023

Study information

• Verified date: June 2023
• Source: Trakya University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Aim: This randomized controlled trial study aimed to evaluate the effect of SMS use on compliance with postoperative breathing and coughing exercises and patient satisfaction in patients undergoing pulmonary lobectomy for lung cancer surgery.

Material and methods: In the study, 62 patients who underwent lobectomy in a university hospital's thoracic surgery clinic between 01.02.2022 and 03.04.2023. The intervention group was chosen to be the group that received SMS messages.

Description:

Background: Patients undergoing lung resection should be encouraged to cough, take deep breaths for pulmonary rehabilitation within the scope of enhanced recovery after surgery protocols. The success of protocols is related to patient compliance. SMS-based interventions increase compliance with medications and protocols in surgical patients and reduce hospital readmission rates, while improving patients' clinical participation and satisfaction.

Aim: This randomized controlled trial study aimed to evaluate the effect of SMS use on compliance with postoperative breathing and coughing exercises and patient satisfaction in patients undergoing pulmonary lobectomy for lung cancer surgery.

Material and methods: In the study, 62 patients who underwent lobectomy in a university hospital's thoracic surgery clinic between 01.02.2022 and 03.04.2023. The intervention group was chosen to be the group that received SMS messages.

"The Information Form", "Postoperative exercise follow-up chart", "Postoperative patient evaluation form" and "Patient satisfaction form were used in data collection. Independent sample t-test, Pearson chi- square and Mann Whitney U test were conducted for statistical analyses.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 62
• Est. completion date: April 3, 2023
• Est. primary completion date: April 3, 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• undergoing elective pulmonary lobectomy,

• having preoperative normal lung capacity (pulmonary function test result FEV1/FVC >70%),

• being compatible with the use of triflow, undergoing pulmonary lobectomy for the first time,

• volunteering to participate in the study,

• having mental competence,

• not having Turkish communication problems,

• having a personal mobile phone and accepting to send SMS,

• being an adult (=18)

Exclusion Criteria:

• If any SMSs are not received during the study period, the patient will be excluded from the study.

Related Conditions & MeSH terms

• Lung Neoplasms
• Pulmonary Cancer
• Surgery

Intervention

Procedure:
• SMS
Receive SMS

Locations

Country	Name	City	State
Turkey	Trakya University	Edi?rne
Turkey	Turkey, Trakya University	Edirne

Sponsors (1)

Lead Sponsor	Collaborator
Trakya University

Country where clinical trial is conducted

Turkey, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	primary outcome measure	The primary point of the study was defined as evaluating the effect of sending SMSs, on compliance with postoperative breathing and coughing exercises undergoing pulmonary lobectomy surgery.A postoperative exercise follow-up chart includes the breathing, coughing, triflow exercises performed by the patients on the 1st and 4th postoperative days and the hours of the exercises. The mean number of breathing and coughing exercises on the first and fourth postoperative days was recorded.	change from after implamentation 1st and 4rd days of operation.
Secondary	secondary outcome measure	The second point of the study was defined as evaluating the effect of sending SMSs, on patient satisfaction undergoing pulmonary lobectomy surgery. "Patient satisfaction form" were used for data collection.The patient satisfaction form" consisted of two questions. The first question questioned the satisfaction with SMS reminders. Satisfaction levels were categorized in 4 ways. Level of "very satisfied" and "satisfied" were accepted as high satisfaction level, "was not satisfied" and "was not satisfied at all" were accepted as low level.	change from after implamentation 4rd days of operation.