Effect of Digital Physiotherapy Practice on Pulmonary Function, Muscle Strength, Quality of Life After Thoracic Surgery

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-75
SponsorBezmialem Vakif University

About this trial

Thoracic surgery is the primary intervention used in the treatment of diseases affecting the lungs, pleura, chest wall, and mediastinum. Postoperative changes occur in both lung functions and clinical symptoms due to the procedure itself and patient-related factors. After thoracic surgery, patients often experience reduced exercise tolerance and impaired respiratory functions, negatively affecting their participation in daily activities, functional levels, and quality of life. In open thoracotomies, the incision site, severed muscles, and the size of the incision can impact upper extremity and trunk functions. The aim of this study is to investigate the effects of physiotherapy applied through digital methods on respiratory functions, respiratory muscle strength, functional capacity, upper extremity muscle strength, and quality of life in patients who have undergone thoracic surgery.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients who underwent open thoracotomy

Agreement to participate in the study

Being between the ages of 18-75

Having an internet connection at home and being able to participate in video-conference sessions via desktop-laptop computers, smartphones, electronic tablets, etc.

Disqualifiers

Pneumonectomy surgeries

Having a cardiac, orthopedic, neurological or systemic disease that would prevent exercise

Having mental, communication or behavioral disorders that would cause problems in understanding commands and questions or performing exercises.

Participating in a pulmonary rehabilitation program before surgery

Trial design

Design model

Parallel

Treatments tested in this trial

  • Exercise

    Other intervention

    Exercise sessions will begin with flexibility exercises targeting the shoulder and neck regions. This will be followed by breathing exercises utilizing fundamental respiratory techniques. Extremity exercises will include movements focused on the upper extremities and trunk, with progression applied according to a pre-established plan. Each session will conclude with cool-down exercises. Additionally, patients will be encouraged to engage in regular walking on a weekly basis.

  • Standard care

    Other intervention

    Patients will receive education regarding the critical aspects to consider after hospital discharge. Standard postoperative care protocols will be implemented.

Treatment groups

26 Participants
are divided into 2 treatment groups
Group A: Training groupActive comparator 1 intervention
Group B: Control groupActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Forced vital capacity (FVC)

The volume of air exhaled during a full and strongest exhalation possible after a full inspiration, as measured by a spirometry device.

Time frame
12 weeks
2

Forced expiratory volume in 1 second (FEV1)

FEV1 is the expiratory volume in the first second of the FVC maneuver.

Time frame
12 weeks
3

Tiffeneau ratio (FEV1/FVC)

The FEV1/FVC represents the fraction of air a patient exhales in the first second. This measurement is crucial for detecting airflow obstruction.

Time frame
12 weeks
4

Peak expiratory flow (PEF)

Peak Expiratory Flow (PEF) is defined as a maximal expiratory flow generated during a simple maneuver using a peak flow meter via a mouthpiece.

Time frame
12 weeks

Secondary outcomes

1

Shoulder Joint Range of Motion Measurement

Change of shoulder flexion and abduction range of motion

Time frame
12 weeks
2

Trunk Lateral Flexion Flexibility

It is the measurement of the distance between the first and last points during lateral flexion of the trunk with a tape measure. (in centimeters)

Time frame
12 weeks
3

Chest Expansion

Evaluation of change in chest expansion. The largest differences between maximum inspiration and maximum expiration is recorded as chest expansion.

Time frame
12 weeks
4

Shoulder Pain

Assessment is made using the Shoulder Pain and Disability Index. Higher scores indicate more severe pain and greater disability.

Time frame
12 weeks

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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