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NCT Number: NCT06965595

The Effect of Different Physiotherapy Methods Applied After Gynecological Abdominal Surgery on Postoperative Symptoms

Gynecological pelvic surgeries include procedures such as myomectomy, hysterectomy, and removal of ovarian cysts performed in the pelvic region of women. In the postoperative period following these surgeries, symptoms such as pain, decreased bowel motility, gastrointestinal problems, nausea, and vomiting are commonly observed. Effective management of these symptoms is important to accelerate the recovery process and improve the quality of life of patients.

This study is planned to evaluate the effectiveness of physiotherapy during the hospitalization period after gynecological abdominal surgery and to examine the effects of different approaches on postoperative symptoms.

In our study, participants who undergo gynecological abdominal surgery and meet the inclusion and exclusion criteria will be divided into four groups for intervention. In addition to routine care, interventions including physiotherapy, vagal stimulation, and a combination of physiotherapy and vagal stimulation will be applied from the postoperative period until discharge. The effects of these interventions on pain, bowel function, autonomic functions, pelvic floor function, and walking will be examined.

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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Nuh Naci Yazgan Unıversıty

Kayseri, Turkey (Türkiye)

About this study

Gynecological pelvic surgeries refer to procedures performed in the pelvic region of women. These surgeries include procedures such as myomectomy, hysterectomy, and the removal of ovarian cysts. Surgical procedures can be performed through abdominal or vaginal routes.

Various complications may occur during or after surgical operations . In the postoperative period, complaints such as pain, decreased bowel motility (e.g., paralytic ileus) , gastrointestinal problems, nausea and vomiting, and pneumonia may occur . At the same time, the occurrence of these complaints may also lead to a decrease in the patient's level of mobility .

There are different treatment approaches for symptoms that occur in the postoperative period. In particular, pain is among the primary complaints of patients. This acute pain may lead to chronic pain and the analgesic agents used may cause side effects such as sedation, nausea, and ileus .

Physiotherapy and rehabilitation practices for gastrointestinal problems and pain in the postoperative period include applications such as breathing exercises, mobilization, and connective tissue massage .

In a study by Zia and colleagues on the effectiveness of early physiotherapy applications, cases who underwent abdominal hysterectomy were divided into two groups as control and experimental. The experimental group received a comprehensive physiotherapy rehabilitation plan including patient education, breathing exercises, early mobilization, connective tissue manipulation, and transcutaneous electrical nerve stimulation (TENS), while the control group only performed walking (ambulation). It was shown that participants in the experimental group had a faster time to first gas passage and a higher rate of defecation within the first 3 days compared to the control group. As a result of the study, it is stated that early postoperative intervention has the potential to accelerate the recovery process .

In another study, the effect of kinesio taping and breathing exercises on pain in cases undergoing gynecological abdominal surgery was examined. The researchers divided the participants into four groups: kinesio taping, breathing exercises, kinesio taping with breathing exercises, and control group, and conducted interventions for 3 days postoperatively. Time to gas passage and defecation times were evaluated, and kinesio taping was found to be the group with the best improvement in pain and the earliest gas passage time. The group that received kinesio taping and breathing exercises also showed shorter gas passage times. As a result, kinesio taping and kinesio taping with breathing exercises can be used as non-invasive methods in the postoperative period .

Recently, the vagal stimulation technique has come to the forefront among applications for pain relief . This method has also been used in individuals with complaints of constipation . Stimulation of the vagus nerve can be provided through invasive and non-invasive methods.

In a study conducted by Shi and colleagues in 2021, 42 patients with constipation-predominant irritable bowel syndrome were divided into two groups and received auricular vagal stimulation and sham vagal stimulation treatments. In this study, which examined constipation and abdominal pain, positive results such as increased bowel motility and reduced pain were obtained after 4 weeks .

In another study involving patients with chronic low back pain, 60 patients were divided into two groups to receive either conventional rehabilitation and home exercises or transcutaneous auricular vagal nerve stimulation and home exercises. At the end of the 3-week treatment program, intra-group evaluation results showed positive effects on mobility, functional status, depression, and sleep in all groups .

This study is planned to evaluate the effectiveness of physiotherapy during the hospitalization period after gynecological abdominal surgery and to examine the effects of different approaches on postoperative symptoms.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Being 18 years of age or older
  • Having undergone surgery due to a gynecological condition
  • Having undergone one of the following operations: hysterectomy, hysterectomy + oophorectomy, or hysterectomy + salpingo-oophorectomy
  • Having undergone abdominal surgery

Exclusion criteria

  • Development of any complications during or after surgery
  • Presence of active malignancy
  • Presence of severe organ failure
  • Presence of uncontrolled cardiac or other systemic disorders
  • Presence of neurological or cognitive diseases

Treatment and study plan

Routine care

Other

This group will be the control group. Routine care practices carried out in the hospital (vital sign monitoring, administration of analgesics, anti-inflammatory and antibiotics when necessary, and mobilization starting from the 6th hour) will be applied and the data will be recorded.

Routine care + Physiotherapy

Other

In addition to routine care practices, this group will receive physiotherapy and rehabilitation. During the postoperative period, the intervention will be applied twice a day.

Posture training: Information about posture will be provided in different positions and training will be conducted.

Breathing training (Diaphragmatic breathing, thoracic expansion exercises)

In-bed mobilization (Lower and upper extremity exercises, foot-ankle exercises (dorsiflexion-plantar flexion / inversion-eversion), hip and knee flexion-extension exercises, cervical region joint range of motion and stretching exercises, upper extremity exercises (shoulder elevation, circumduction, elbow and wrist flexion-extension exercises), pelvic floor training and exercises)

Out-of-bed mobilization (Sitting, standing, walking training after the 6th hour)

Routine care + Vagal stimulation

Other

In addition to routine care practices, this group will receive vagal stimulation. The stimulation will be applied to the cervical region at 10 Hz, 200 μs for 20 minutes, twice a day.

Routine care + Physiotherapy + Vagal stimulation

Other

In addition to routine care practices, this group will receive physiotherapy and rehabilitation, along with vagal stimulation.

Primary outcomes

  1. Postoperative Pain (VAS)

    Time frame: Day 1 and Day 2

    Pain will be assessed before and after each session. Visual Analog Scale (VAS) will be used for this. Minimum value is 0 and max value is 10. Ten is a higher pain. Zero means no pain.

  2. Pain threshold measurement

    Time frame: Baseline and Day 2

    A digital algometer device will be used to determine the pain threshold.

  3. Assessment of Autonomic Functions

    Time frame: Day 1 and Day 2

    The recording will be made with an ECG device.R-R waves will be examined.

  4. Assessment of Autonomic Functions

    Time frame: Day 1 and Day 2

    heart rate collected before and after the session.

  5. Assessment of Autonomic Functions

    Time frame: Day 1 and Day 2

    Blood Pressure collected before and after the session.

  6. Assessment of Autonomic Functions

    Time frame: Day 1 and Day 2

    respiratory rate collected before and after the session.

  7. Assessment of saturation (SpO₂)

    Time frame: Day 1 and Day 2

    arterial oxygen saturation (SpO₂) levels of participants will be evaluated. The unit of measurement will be the percentage of oxygen saturation.

  8. Postoperative period

    Time frame: From enrollment to the end of treatment at 2 day

    The time when the first feeling of needing to pass gas time and defecation occurs will be noted.

  9. The walking time

    Time frame: Postoperative

    The time of first walking will be noted.

  10. First food intake

    Time frame: Postoperative

    The time of First food intake will be noted.

  11. Take a medicine

    Time frame: Day 1 and Day 2

    Analgesics and other medications taken will be noted.

  12. Umblikus

    Time frame: Day 1 and Day 2

    Umbilicus circumference will be measured with a tape measure.

  13. xiphoid - pubis distance

    Time frame: day 1 and day 2

    The distance between the xiphoid and pubis will be measured with a tape measure. It will be noted in cm.

  14. Postoperative period

    Time frame: Postoperative

    The time when the first feeling of needing to urinate occurs and the time when the feeling of micturition occurs will be noted.

Secondary outcomes

  1. DETAILED STORIES OF THE PATIENTS

    Time frame: Before treatment

    Participants' age, height, weight, number and status of pregnancies (gravida, abortus, dilation & curettage, parity, number of living children, etc.), previous surgeries, medications used, comorbidities, chronic diseases, marital status, and current type of surgery will be assessed.

    Medical history, personal and family medical background, BMI, smoking habits, other lifestyle habits, and allergy status will also be evaluated.

  2. Two minutes walk

    Time frame: Day 1 and Day 2

    The distance she can walk in two minutes will be recorded

  3. Pelvic Floor

    Time frame: Day 1 and Day 2

    To assess the condition of the pelvic floor, researchers will evaluate it using the Visual Analog Scale (VAS). This assessment will address whether the participant can feel the pelvic region, as well as the presence of pain, discomfort, or incontinence. Min value is 0 . It means no sense and max value is 10. It means high score for question.

  4. Pelvic Floor Distress Inventory-20 (PFDI-20)

    Time frame: Day1 and Day 2

    Pelvic floor symptoms will be evaluated using the Pelvic Floor Distress Inventory-20 (PFDI-20), which includes a separate subheading for these symptoms.The higher the score obtained from this questionnaire, the greater the degree of complaints about pelvic floor dysfunction.

  5. Quality of Recovery-40

    Time frame: Day 1 and Day 2

    It will be used to examine the recovery characteristics of the participants throughout the treatment process.Higher scores indicating higher levels of functioning or well-being.

  6. Respiratory Function Test

    Time frame: Day 1 and Day 2

    It will be used to assess the patient's respiratory capacity.

  7. Patient Satisfaction

    Time frame: Day 2

    Their satisfaction with the treatment will be evaluated.Minimum value is 0 and max value is 10. Ten is a higher satisfaction. Zero means no satisfaction.

  8. Mini Mental Test

    Time frame: Before treatment

    It will be used to evaluate the cognitive status item included in the exclusion criteria.

  9. Operation process

    Time frame: Baseline

    Information regarding the surgery (duration and time) will be noted.

Sponsors and collaborators

Lead sponsor

Hacettepe University

Other

Collaborators

  • Nuh Naci Yazgan University

Registry information

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
May 11, 2025
Registry last updated
Aug 1, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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