CompletedNot Applicable

Effect of SMS Use on Postoperative Respiratory and Cough Exercise Compliance

Turkey (Türkiye)62 participantsStarted 2022-02-01

Plain-language 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.

Who can participate

Age range

18 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

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.

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

primary outcome measure

Timeframe: change from after implamentation 1st and 4rd days of operation.

Trial details

NCT IDNCT05915221

SponsorTrakya University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2023-04-03

View on ClinicalTrials.gov More Pulmonary Cancer trials