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Postoperative Pulmonary ComplicationsTEACH-BREATHENCT07350616

The Effect of the 5T Teach-Back Method on Respiratory Exercise and Incentive Spirometer Training

A study testing 5T Teach-Back-Based Respiratory Exercise and Incentive Spirometer Education and Standard Verbal Respiratory Education in people with Postoperative Pulmonary Complications and Atelectasis, run by Suleyman Demirel University.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

Breathing problems after surgery are common and can lead to serious complications such as low oxygen levels, lung collapse, or pulmonary embolism. These problems increase patient risk and place an additional burden on the healthcare system. Read more about this study

Who is it for?
Ages 18 years and older
What is being tested?
5T Teach-Back-Based Respiratory Exercise and Incentive Spirometer Education and Standard Verbal Respiratory Education
Could I receive a placebo?
No, everyone receives an active treatment
How many people
76 participants
Where
No sites listed yet
Study dates
15 Jan 2026to 15 Jan 2027
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Adults aged 18 years or older
  • Scheduled for abdominal surgery under general anesthesia
  • Postoperative use of respiratory exercises and incentive spirometry is recommended
  • Expected postoperative hospital stay of more than 3 days
  • Able to read and write and able to communicate effectively
  • Conscious, cooperative, and oriented
  • Willing to participate voluntarily and able to provide written informed consent

Who cannot join

  • Severe neurological or cognitive impairment
  • Unstable vital signs or hemodynamic instability
  • Anticipated or required postoperative intensive care unit admission
  • Severe pain that prevents participation in education or assessments
  • Visual or communication impairments that limit participation in education

Trial locations and contacts

No sites are listed yet. Contact the study team or a site near you to ask about taking part.

Cigdem Erdem, Assistant Professor contact

+095075011397

cgdmctn07@gmail.com

About this study

Official title: The Effect of the 5T Teach-Back Method in Respiratory Exercise and Incentive Spirometer Training on Knowledge Level, Practical Skills, Respiratory Parameters, and Patient Satisfaction: A Randomized Controlled Study

Breathing problems after surgery are common and can lead to serious complications such as low oxygen levels, lung collapse, or pulmonary embolism. These problems increase patient risk and place an additional burden on the healthcare system. Breathing exercises and incentive spirometer use are important methods to prevent these complications. However, many patients have difficulty understanding and correctly performing these exercises when education is limited to standard verbal instructions. This randomized controlled study aims to evaluate whether the 5T Teach-Back education method improves patients' understanding, practical skills, respiratory outcomes, and satisfaction compared with standard verbal education. The study will be conducted in a university hospital and will include 76 adult patients undergoing abdominal surgery under general anesthesia. Participants will be randomly assigned to either an intervention group or a control group.

Patients in the intervention group will receive preoperative breathing exercise and incentive spirometer training using the 5T Teach-Back method, which encourages patients to explain the information back in their own words and repeat the skills until they are correctly understood. Patients in the control group will receive routine verbal education provided by clinical nurses. Outcomes will be measured before surgery and again within 24-72 hours after surgery. These outcomes include patients' knowledge level, correct performance of breathing exercises and spirometer use, respiratory rate, oxygen saturation, lung function test results, and patient satisfaction with nursing care. The results of this study are expected to show whether the 5T Teach-Back method is more effective than standard education in improving postoperative respiratory care and patient satisfaction. The findings may help standardize patient education practices and support nurses in delivering more effective respiratory training before surgery.

Being tested
5T Teach-Back-Based Respiratory Exercise and Incentive Spirometer Education, Standard Verbal Respiratory Education
Medical subject headings
Pulmonary Atelectasis

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • 5T Teach-Back-Based Respiratory Exercise and Incentive Spirometer EducationBehavioural

    This intervention involves preoperative respiratory exercise and incentive spirometer education delivered using the structured 5T Teach-Back method. Education is provided individually by a trained nurse and includes demonstration, patient return demonstration, and repeated instruction until correct understanding and performance are achieved. The five steps of the 5T Teach-Back approach (Triage, Tools, Take Responsibility, Tell Me, and Try Again) are systematically applied to ensure patient comprehension and skill mastery. Sessions last approximately 20-30 minutes and are completed before surgery. Unlike routine verbal education, this intervention actively engages patients in explaining and performing the exercises in their own words, allowing immediate correction of misunderstandings and reinforcing correct technique

  • Standard Verbal Respiratory EducationBehavioural

    This intervention consists of routine verbal education on respiratory exercises and incentive spirometer use provided by clinical nurses as part of standard preoperative care. Education is delivered according to usual clinical practice without a structured teaching framework, return demonstration, or formal assessment of patient understanding. No standardized duration, repetition, or feedback process is applied. This intervention reflects typical routine care and differs from structured educational approaches by relying solely on conventional verbal instruction.

Study groups in NCT07350616
Study groupRoleWhat they receive
5T Teach-Back Education GroupExperimentalParticipants receive preoperative respiratory exercise and incentive spirometer training using the 5T Teach-Back method.
Receives: Behavioral: 5T Teach-Back-Based Respiratory Exercise and Incentive Spirometer Education
Standard Education GroupActive comparatorParticipants receive routine verbal education on respiratory exercises and incentive spirometer use provided by clinical nurses.
Receives: Behavioral: Standard Verbal Respiratory Education

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Patient Knowledge and Correct Performance of Respiratory Exercises and Incentive Spirometer Use

    Patient knowledge and correct performance of respiratory exercises and incentive spirometer use will be assessed using a structured knowledge test and observation-based checklists. Knowledge level will be evaluated with a short multiple-item test, and performance accuracy will be assessed by direct observation of breathing exercises and incentive spirometer use. Higher scores indicate better understanding and correct application of the techniques.

    Measured: From baseline (preoperative period) to 24-72 hours postoperatively

Secondary outcomes (4)
  1. Pulmonary Function Test

    Pulmonary function will be assessed postoperatively using spirometry. The primary parameter will be the FEV1/FVC ratio (%), where higher values indicate better pulmonary function.

    Measured: 24-72 hours postoperatively

  2. Patient Satisfaction

    Patient satisfaction will be assessed using the Newcastle Satisfaction with Nursing Scales (NSNS). The NSNS was originally developed by Thomas et al. (1996) to evaluate patients' experiences and satisfaction with nursing care and was adapted and validated in Turkish by Akın and Erdoğan (2007). The scale consists of 19 items rated on a 5-point Likert scale. Item scores are summed and transformed to yield a total satisfaction score ranging from 0 to 100. Higher scores indicate greater satisfaction with nursing care, with a score of 100 representing the highest possible level of satisfaction.

    Measured: 24-72 hours postoperatively

  3. Respiratory Parameter (SpO₂)

    Peripheral oxygen saturation (SpO₂, %) will be measured pulse oximetry. Changes between baseline (preoperative) and postoperative assessment will be compared between study group

    Measured: From baseline (preoperative period) to 24-72 hours postoperatively

  4. Respiratory Rate

    Respiratory rate (breaths/min) will be measured using routine clinical assessment. Changes between baseline (preoperative period) and postoperative assessment will be compared between study groups.

    Measured: From baseline (preoperative period) to 24-72 hours postoperatively

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted20 Jan 2026
  2. Study start15 Jan 2026 (estimated)
  3. Primary completion15 Jan 2027 (estimated)
  4. Study completion15 Jan 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Prevention
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Participant
Enrolment
76 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07350616
Sponsor's protocol ID
973-973-11
Acronym
TEACH-BREATHE
Status last verified
Jan 2026
First submitted
28 Dec 2025
Last updated
20 Jan 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Wang J, Hu H, Sun J, Zhang Q, Chen Z, Wang Q, Zhu M, Yao J, Yuan H, Zhang X. The effectiveness of health education based on the 5Ts for teach-back on oral nutritional supplements compliance of post-discharge patients after surgery for gastric cancer: a randomized controlled trial. Support Care Cancer. 2023 Feb 11;31(3):157. doi: 10.1007/s00520-023-07581-1.

    PubMed 36773116
  • Anderson KM, Leister S, De Rego R. The 5Ts for Teach Back: An Operational Definition for Teach-Back Training. Health Lit Res Pract. 2020 Apr 9;4(2):e94-e103. doi: 10.3928/24748307-20200318-01.

    PubMed 32293689

Questions about this trial

What is this clinical trial studying?

A study testing 5T Teach-Back-Based Respiratory Exercise and Incentive Spirometer Education and Standard Verbal Respiratory Education in people with Postoperative Pulmonary Complications and Atelectasis, run by Suleyman Demirel University.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 7 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 20 Jan 2026. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Cigdem Erdem, Assistant Professor (+095075011397, cgdmctn07@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Patient Knowledge and Correct Performance of Respiratory Exercises and Incentive Spirometer Use (time frame: From baseline (preoperative period) to 24-72 hours postoperatively). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT07350616, which also lists 2 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 20 Jan 2026; AzTrials last refreshed its copy on 6 Nov 2026.

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