Pelvic Floor Disorders
Conditions
Brief summary
Currently, perioperative pelvic floor physical therapy (PFPT) is not standard of care for all patients who undergo vaginoplasty surgery. While some practices have implemented these new programs, and the above data exist on outcomes associated with perioperative PFPT in transgender women undergoing vaginoplasty, no study has compared implementation of perioperative PFPT to routine care (no perioperative PFPT). Therefore, the primary objective of this study was to compare the effectiveness of postoperative PFPT compared to no PFPT in transgender women undergoing vaginoplasty surgery for gender affirmation. Secondary objectives of the study are 1) to describe the incidence of preoperative pelvic floor dysfunction in transgender women undergoing PFPT and 2) to compare the effectiveness of postoperative PFPT alone to pre- and postoperative PFPT in these patients.
Detailed description
This was a randomized double-blind study. Both subjects and the surgeon performing the surgery as well as the personnel administering questionnaires to patients postoperatively were blinded to the randomization. Recruitment, Enrollment and Randomization Patients scheduled to undergo vaginoplasty surgery at Cleveland Clinic Main campus were approached about voluntary participation in this study. This occurred over the phone approximately one to three months before their scheduled surgery. Patients who agreed to participate were sent a consent form via the mail and were asked to sign consent in person. Enrollment and randomization occurred following informed consent. All patients were given a copy of their signed and dated consent. Once enrolled, patients were randomized into one of two groups: * Postoperative PFPT * No Postoperative PFPT If patients were randomized into the Postoperative PFPT arm, they were further randomized into the following sub-arms: * Postoperative PFPT alone * Preoperative and Postoperative PFPT Surgery: All patients underwent vaginoplasty surgery by a single surgeon in a standard fashion. The neovaginal cavity was created using the same technique across all patients. Postoperative care was routine and the same for all patients. Postoperative Pelvic Floor Physical Therapy: There was three possible PFPT regimens. All PT regimens were performed by the same two physical therapists, trained in the management of patients who have undergone vaginoplasty surgery. 1. No PFPT Patients were present to see the physical therapist 3 weeks postoperatively. The following interventions were performed: Subjective assessment of bowel and bladder function. Visual and external palpation and assessment of external pelvic floor region. Intravaginal pelvic floor assessment. Pelvic floor muscle dynamics and coordination assessment. Review of pelvic floor anatomy and function. 2. Postoperative PFPT Only Patients presented to the physical therapist 3 weeks and 6 weeks postoperatively. The following interventions were performed: 3 weeks: * Subjective assessment of bowel and bladder function * Visual and external palpation and assessment of external pelvic floor region * Intravaginal pelvic floor assessment * Pelvic floor muscle dynamics and coordination assessment * Instruction of pelvic floor coordination and lengthening * Discussion of dilator program and progression * Home program with instructions 6 weeks: * External scar assessment and treatment if tissue healing allows * Instruction to patient of scar mobilizations * Intravaginal pelvic floor assessment and treatment if indicated * Review of pelvic floor lengthening and coordination * Review and progression of dilator program if appropriate * Assessment of current bowel/bladder symptoms; home program and instructions to address these symptoms 3\) Preoperative PFPT and Postoperative PFPT: Patients presented to see the physical therapist 3 weeks before surgery, 3 weeks and 6 weeks postoperatively. The following interventions were performed: Preoperative: * Diaphragmatic breathing * Discuss dilator positioning/introduce dilator program * External pelvic floor assessment * Teach pelvic floor coordination * Assessment of current bowel/bladder symptoms; home program and instructions to address these symptoms 3 weeks: * Subjective assessment of bowel and bladder function * Visual and external palpation and assessment of external pelvic floor region * Intravaginal pelvic floor assessment * Pelvic floor muscle dynamics and coordination assessment * Instruction of pelvic floor coordination and lengthening * Discussion of dilator program and progression * Home program with instructions 6 weeks: * External scar assessment and treatment if tissue healing allows * Instruction to patient of scar mobilizations * Intravaginal pelvic floor assessment and treatment if indicated * Review of pelvic floor lengthening and coordination * Review and progression of dilator program if appropriate * Assessment of current bowel/bladder symptoms; home program and instructions to address these symptoms Study Questionnaires & Exams: All patients were administered questionnaires preoperatively and 12 weeks postoperatively. The following questionnaires were administered: Preoperatively: * CRAD-8 and UDI-6 * PFIQ-7 Postoperatively 1 week (at the time of routine dilation teaching): • Vaginal length (routine exam) Postoperatively 12 weeks: * CRAD-8 and UDI-6 * PFIQ-7 * PGI-I * Ease of Passing Dilator (VAS 0-10) * Pain with Dilation (VAS 0-10) * Largest dilator size used * Vaginal length (routine exam) Cross-Over Treatment: Any patients in the No PFPT arm who were determined to have pelvic floor dysfunction or symptoms that may have benefitted from PFPT referral, were referred after the 12-week mark. Any patient in one of the PFPT arms who was determined to still need PFPT for persistent pelvic floor dysfunction or symptoms were referred for continued care.
Interventions
Patients will present to see the physical therapist 3 weeks and 6 weeks postoperatively. The following interventions will be performed: 3 weeks: * Subjective assessment of bowel and bladder function * Visual and external palpation and assessment of external pelvic floor region * Intravaginal pelvic floor assessment * Pelvic floor muscle dynamics and coordination assessment * Instruction of pelvic floor coordination and lengthening * Discussion of dilator program and progression * Home program with instructions 6 weeks: * External scar assessment and treatment if tissue healing allows * Instruction to patient of scar mobilizations * Intravaginal pelvic floor assessment and treatment if indicated * Review of pelvic floor lengthening and coordination * Review and progression of dilator program if appropriate * Assessment of current bowel/bladder symptoms; home program and instructions to address these symptoms
Patients will present to see the physical therapist 3 weeks postoperatively. The following interventions will be performed: Subjective assessment of bowel and bladder function. Visual and external palpation and assessment of external pelvic floor region. Intravaginal pelvic floor assessment. Pelvic floor muscle dynamics and coordination assessment. Review of pelvic floor anatomy and function.
Preoperative Diaphragmatic breathing Discuss dilator positioning/introduce dilator program External pelvic floor assessment Teach pelvic floor coordination Current bowel/bladder symptoms; home program and instructions 3 weeks Assessment of bowel and bladder function Visual and external palpation and assessment of external pelvic floor region Intravaginal pelvic floor assessment Pelvic floor muscle dynamics and coordination assessment Instruction of pelvic floor coordination and lengthening Discussion of dilator program and progression Home program with instructions 6 weeks External scar assessment and treatment if tissue healing allows Instruction to patient of scar mobilizations Intravaginal pelvic floor assessment and treatment if indicated Review of pelvic floor lengthening and coordination Review and progression of dilator program if appropriate Current symptoms; home program and instructions
Sponsors
Study design
Eligibility
Inclusion criteria
* Age greater than or equal to 18 years of age * Patients scheduled for full-depth vaginoplasty surgery
Exclusion criteria
* Inability to speak or comprehend the English language * Patients scheduled for no-depth vaginoplasty surgery * Patients who have undergone previous PFPT * Patients who are s/p prostatectomy or treatment for prostate cancer
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Patient Reported Ease of Dilation | 12 weeks | VAS 0-10 is a validated 10 item questionnaire. Responses to each question are scored on a 10-point Likert scale, ranging from 0 (no pain) to 10 (worst pain). A response of 10 is considered to be a worse outcome. |
Countries
United States
Participant flow
Participants by arm
| Arm | Count |
|---|---|
| Postoperative Pelvic Floor Physical Therapy (PFPT) Pelvic Floor Physical Therapy (PFPT): Patients will present to see the physical therapist 3 weeks and 6 weeks postoperatively. The following interventions will be performed:
3 weeks:
* Subjective assessment of bowel and bladder function
* Visual and external palpation and assessment of external pelvic floor region
* Intravaginal pelvic floor assessment
* Pelvic floor muscle dynamics and coordination assessment
* Instruction of pelvic floor coordination and lengthening
* Discussion of dilator program and progression
* Home program with instructions
6 weeks:
* External scar assessment and treatment if tissue healing allows
* Instruction to patient of scar mobilizations
* Intravaginal pelvic floor assessment and treatment if indicated
* Review of pelvic floor lengthening and coordination
* Review and progression of dilator program if appropriate
* Assessment of current bowel/bladder symptoms; home program and instructions to address these symptoms | 10 |
| No Postoperative Pelvic Floor Physical Therapy (PFPT) Patients will present to see the physical therapist 3 weeks postoperatively. The following interventions will be performed: Subjective assessment of bowel and bladder function. Visual and external palpation and assessment of external pelvic floor region. Intravaginal pelvic floor assessment. Pelvic floor muscle dynamics and coordination assessment. Review of pelvic floor anatomy and function.
No Pelvic Floor Physical Therapy (PFPT): Patients will present to see the physical therapist 3 weeks postoperatively. The following interventions will be performed:
Subjective assessment of bowel and bladder function. Visual and external palpation and assessment of external pelvic floor region. Intravaginal pelvic floor assessment. Pelvic floor muscle dynamics and coordination assessment. Review of pelvic floor anatomy and function.
Cross-over Treatment: Any patients in the No PFPT arm who are determined to have pelvic floor dysfunction or symptoms that may benefit from PFPT referral, will be referred after the 12-week mark. Any patient in one of the PFPT arms who is determined to still need PFPT for persistent pelvic floor dysfunction or symptoms will be referred for continued care. | 17 |
| Pre and Postoperative Pelvic Floor Physical Therapy (PFPT) Pelvic Floor Physical Therapy (PFPT): Patients will present to see the physical therapist within 4 weeks preceding surgery and 3 weeks and 6 weeks postoperatively. The following interventions will be performed:
Preoperative:
Teaching about the pelvic floor and breathing exercises
3 weeks:
* Subjective assessment of bowel and bladder function
* Visual and external palpation and assessment of external pelvic floor region
* Intravaginal pelvic floor assessment
* Pelvic floor muscle dynamics and coordination assessment
* Instruction of pelvic floor coordination and lengthening
* Discussion of dilator program and progression
* Home program with instructions
6 weeks:
* External scar assessment and treatment if tissue healing allows
* Instruction to patient of scar mobilizations
* Intravaginal pelvic floor assessment and treatment if indicated
* Review of pelvic floor lengthening and coordination
* Review and progression of dilator program if appropriate
* Assessment of current bowel/bladder symptoms; home program and instructions to address these symptoms | 10 |
| Total | 37 |
Baseline characteristics
| Characteristic | No Postoperative Pelvic Floor Physical Therapy (PFPT) | Pre and Postoperative Pelvic Floor Physical Therapy (PFPT) | Total | Postoperative Pelvic Floor Physical Therapy (PFPT) |
|---|---|---|---|---|
| Age, Categorical <=18 years | 0 Participants | 0 Participants | 0 Participants | 0 Participants |
| Age, Categorical >=65 years | 0 Participants | 0 Participants | 0 Participants | 0 Participants |
| Age, Categorical Between 18 and 65 years | 17 Participants | 10 Participants | 37 Participants | 10 Participants |
| Age, Continuous | 28 Years STANDARD_DEVIATION 14 | 36 Years STANDARD_DEVIATION 15 | 32.3 Years STANDARD_DEVIATION 12 | 33 Years STANDARD_DEVIATION 7 |
| Race (NIH/OMB) American Indian or Alaska Native | 0 Participants | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Asian | 0 Participants | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Black or African American | 3 Participants | 1 Participants | 5 Participants | 1 Participants |
| Race (NIH/OMB) More than one race | 0 Participants | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Native Hawaiian or Other Pacific Islander | 0 Participants | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Unknown or Not Reported | 0 Participants | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) White | 14 Participants | 9 Participants | 32 Participants | 9 Participants |
| Region of Enrollment United States | 17 participants | 10 participants | 37 participants | 10 participants |
| Sex: Female, Male Female | 17 Participants | 10 Participants | 37 Participants | 10 Participants |
| Sex: Female, Male Male | 0 Participants | 0 Participants | 0 Participants | 0 Participants |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk | EG002 affected / at risk |
|---|---|---|---|
| deaths Total, all-cause mortality | 0 / 10 | 0 / 17 | 0 / 10 |
| other Total, other adverse events | 0 / 10 | 0 / 17 | 0 / 10 |
| serious Total, serious adverse events | 0 / 10 | 0 / 17 | 0 / 10 |
Outcome results
Patient Reported Ease of Dilation
VAS 0-10 is a validated 10 item questionnaire. Responses to each question are scored on a 10-point Likert scale, ranging from 0 (no pain) to 10 (worst pain). A response of 10 is considered to be a worse outcome.
Time frame: 12 weeks
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Postoperative Pelvic Floor Physical Therapy (PFPT) | Patient Reported Ease of Dilation | 6.6 units on a scale | Standard Deviation 1.9 |
| No Postoperative Pelvic Floor Physical Therapy (PFPT) | Patient Reported Ease of Dilation | 7.4 units on a scale | Standard Deviation 1.7 |
| Preoperative and Postoperative Pelvic Floor Physical Therapy (PFPT) | Patient Reported Ease of Dilation | 8.0 units on a scale | Standard Deviation 0.8 |
Mean Difference in CRADI-8 Score
Colorectal-Anal Distress Inventory (CRADI-8) provides a symptom inventory (no or yes) and if yes (to measure the degree of bother and distress) caused by the broad array of pelvic floor symptoms, in particular colorectal-anal distress. Responses to the eight questions are scored on a 4-point Likert scale, ranging 1 (not at all) to 4 (quite a bit). The scale scores are found individually by calculating the mean value of their corresponding questions and then multiplying by 25 to obtain a value that ranges from 0 to 100. The reported outcome for this trial is the mean difference in score. A higher CRADI-8 score indicates a greater level of disability. It reflects more significant challenges in daily activities and functioning. A score of 100 is considered to be a worse outcome.
Time frame: 12 weeks
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Postoperative Pelvic Floor Physical Therapy (PFPT) | Mean Difference in CRADI-8 Score | -0.6 units on a scale | Standard Deviation 3.69 |
| No Postoperative Pelvic Floor Physical Therapy (PFPT) | Mean Difference in CRADI-8 Score | -3.00 units on a scale | Standard Deviation 7.37 |
| Preoperative and Postoperative Pelvic Floor Physical Therapy (PFPT) | Mean Difference in CRADI-8 Score | -1.9 units on a scale | Standard Deviation 7.58 |
Mean Difference in PFIQ-7-Rectum Score
The Pelvic Floor Impact Questionnaire-7 (PFIQ-7) is a seven-question survey that measures the impact of pelvic floor disorders on quality of life, daily activities, and emotional health. The PFIQ-7 is scored on a scale of 0-300. The mean of each of the three scales is calculated, ranging from 0-3. Each mean is multiplied by 100 and then divided by 3. The scale scores are added together to get the total PFIQ-7 score. The reported outcome measure in this trial is the mean difference in this score pre- and post-intervention. A score of 300 is considered to be a worse outcome.
Time frame: 12 weeks
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Postoperative Pelvic Floor Physical Therapy (PFPT) | Mean Difference in PFIQ-7-Rectum Score | 6.2 units on a scale | Standard Deviation 23.21 |
| No Postoperative Pelvic Floor Physical Therapy (PFPT) | Mean Difference in PFIQ-7-Rectum Score | -3.17 units on a scale | Standard Deviation 11.31 |
| Preoperative and Postoperative Pelvic Floor Physical Therapy (PFPT) | Mean Difference in PFIQ-7-Rectum Score | 0.5 units on a scale | Standard Deviation 3.69 |
Mean Difference in PFIQ-7-Vagina Score
The Pelvic Floor Impact Questionnaire-7 (PFIQ-7) is a seven-question survey that measures the impact of pelvic floor disorders on quality of life, daily activities, and emotional health. The PFIQ-7 is scored on a scale of 0-300. The mean of each of the three scales is calculated, ranging from 0-3. Each mean is multiplied by 100 and then divided by 3. The scale scores are added together to get the total PFIQ-7 score. The reported outcome measure in this trial is the mean difference in this score pre- and post-intervention. A higher PFIQ-7 score indicates a greater level of disability. It reflects more significant challenges in daily activities and functioning. A score of 300 is considered to be a worse outcome.
Time frame: 12 weeks
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Postoperative Pelvic Floor Physical Therapy (PFPT) | Mean Difference in PFIQ-7-Vagina Score | 6.3 units on a scale | Standard Deviation 27.65 |
| No Postoperative Pelvic Floor Physical Therapy (PFPT) | Mean Difference in PFIQ-7-Vagina Score | 5.65 units on a scale | Standard Deviation 18.18 |
| Preoperative and Postoperative Pelvic Floor Physical Therapy (PFPT) | Mean Difference in PFIQ-7-Vagina Score | 3.5 units on a scale | Standard Deviation 15 |
Mean Difference PFIQ-7-Bladder Score
The Pelvic Floor Impact Questionnaire-7 (PFIQ-7) is a seven-question survey that measures the impact of pelvic floor disorders on quality of life, daily activities, and emotional health. The PFIQ-7 is scored on a scale of 0-300. The mean of each of the three scales is calculated, ranging from 0-3. Each mean is multiplied by 100 and then divided by 3. The scale scores are added together to get the total PFIQ-7 score. The reported outcome measure in this trial is the mean difference in this score pre- and post-intervention. A higher PFIQ-7 score indicates a greater level of disability. It reflects more significant challenges in daily activities and functioning. A score of 300 is considered to be a worse outcome.
Time frame: 12 weeks
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Postoperative Pelvic Floor Physical Therapy (PFPT) | Mean Difference PFIQ-7-Bladder Score | 6.7 units on a scale | Standard Deviation 22.99 |
| No Postoperative Pelvic Floor Physical Therapy (PFPT) | Mean Difference PFIQ-7-Bladder Score | -1.64 units on a scale | Standard Deviation 10.45 |
| Preoperative and Postoperative Pelvic Floor Physical Therapy (PFPT) | Mean Difference PFIQ-7-Bladder Score | -4.8 units on a scale | Standard Deviation 18.4 |
Mean Difference UDI-6 Score
Urinary Distress Inventory (UDI-6) - The UDI-6 is a 6-item questionnaire. Each item is scored on a scale of 0 to 3, with 0 being not at all and 3 being greatly. The average score is calculated and multiplied by 33 1/3 to give a score on a scale of 0 to 100. A higher score indicates a higher level of disability. The outcome measure reported in this trial is the mean difference in scores pre- and post-intervention. A higher UDI-6 score indicates a greater level of disability. It reflects more significant challenges in daily activities and functioning. A score of 100 is considered to be a worse outcome.
Time frame: 12 weeks
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Postoperative Pelvic Floor Physical Therapy (PFPT) | Mean Difference UDI-6 Score | -1.5 units on a scale | Standard Deviation 14.6 |
| No Postoperative Pelvic Floor Physical Therapy (PFPT) | Mean Difference UDI-6 Score | -1.41 units on a scale | Standard Deviation 7.14 |
| Preoperative and Postoperative Pelvic Floor Physical Therapy (PFPT) | Mean Difference UDI-6 Score | -6.5 units on a scale | Standard Deviation 32.02 |
Severity of Pelvic Floor Dysfunction Based on PGI-I
The Patient Global Impression of Improvement (PGI-I) is a transition scale that is a single question asking the patient to rate their urinary tract condition now, as compared with how it was prior to before beginning treatment on a scale from 1 (very much better) to 7 (very much worse). A score of 7 is considered to be a worse outcome.
Time frame: 12 weeks
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Postoperative Pelvic Floor Physical Therapy (PFPT) | Severity of Pelvic Floor Dysfunction Based on PGI-I | 1.4 units on a scale | Standard Deviation 0.7 |
| No Postoperative Pelvic Floor Physical Therapy (PFPT) | Severity of Pelvic Floor Dysfunction Based on PGI-I | 1.65 units on a scale | Standard Deviation 1.49 |
| Preoperative and Postoperative Pelvic Floor Physical Therapy (PFPT) | Severity of Pelvic Floor Dysfunction Based on PGI-I | 1.9 units on a scale | Standard Deviation 1.3 |