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Educational Program Plus Physiotherapy After Prostatectomy

Primary Purpose

Prostate Cancer, Side Effects

Status
Unknown status
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
Therapeutic educational program
PFMT
TTNS
Sponsored by
University of Alcala
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Prostate Cancer

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Men had undergone radical robotic prostate surgery.
  • Men reading, understanding and freely signing an informed consent form.

Exclusion Criteria:

  • Participants who had received adjuvant therapies (chemotherapy, radiotherapy) before pelvic-perineal physical therapy treatment.
  • Men with a history of pelvic organ surgery.
  • Men with chronic diseases that affects their quality of life.
  • Participants with psychiatric or neurological problems.
  • Postoperative men with cognitive limitations to understand information, respond to questionnaires, consent and / or participate in the study.

Sites / Locations

  • University of Alcalá. FPSM research group. HUPARecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Educational program & pelvic floor muscle training

PFMT group

Arm Description

The educational strategy will consist of explaining a healthy lifestyle guide with videos, mobile apps and activities about the anatomy of the pelvic floor and the physiology of the pelvic organs. It will be recommended to avoid risk factors, such as gaining weight, high impact sports, constipation, smoking, or drinking too much caffeine and alcohol. They will also instruct in toilet habits. The pelvic floor muscle training (PFMT) protocol will be applied. Participants will perform exercises with anal biofeedback, perineal and erectile dysfunction electrotherapy protocol and surface electromyography. They will perform PFMT in supine position, sitting, standing and walking. The intervention will last 5 weeks, 2 sessions per week. Each session will last 30/40 minutes. If the patients have overactive bladder symptoms they will perform transcutaneous tibial nerve stimulation (TTNS) protocol. The intervention will last 5 weeks, 2 sessions per week. Each session will last 30 minutes.

They will receive a basic behavioral educational strategy in the first session including pelvic anatomy and physiology, recommendations to avoid risk factors and toilet habits. The PFMT protocol will be applied. Participants will perform PFMT exercises with anal biofeedback, perineal and erectile dysfunction electrotherapy protocol and surface electromyography. They will perform PFMT in supine position, sitting, standing and walking. The intervention will last 5 weeks, 2 sessions per week. Each session will last 30/40 minutes. If the patients have overactive bladder symptoms they will perform transcutaneous tibial nerve stimulation (TTNS) protocol. The intervention will last 5 weeks, 2 sessions per week. Each session will last 30 minutes.

Outcomes

Primary Outcome Measures

Change in QoL
It will be assessed by Short Form 12 (SF-12) Spanish version. The SF-12 consist in 12 items of 8 dimensions: 2 items about physical function, 1 item about social function, 2 items about physical role, 2 items about emotional role, 2 items about mental health, 1 item about vitality, 1 items about body pain, 1 item about general health. The 8 dimensions are scored from 0 (bad health) to 100 (optimal state of health).
Change in UI
It will be assessed by International Consultation on Incontinence Questionnaire Urinary Incontinence (ICIQ-UI) Spanish version. The ICIQ-UI SF consist in 3 items (Frequency, Quantity and Impact) and 8 questions to identify the UI type. The 3 items are scored from 0 (no incontinence) to 21 (severe incontinence). It will be assessed by 1 hour Pad Test. The Pad test consists in weigh a compress after being used under standardized conditions.
Change in Prostatic Symptoms
It will be assessed by International Prostate Symptom Score (IPSS) Spanish version. The IPSS consist of 6 items plus one about quality of life. The 6 items are scored from 1-7 (mild symptomatology), 8-19 (moderate symptomatology) to 20-35 (severe symptomatology).The item about quality of life is measured qualitatively.
Change in Pelvic Floor Muscle Strength
The measuring consists of 4 factors: strength, relax, endurance and repeatability. It will be measured with manometry (mmHg).
Change in ED
It will be assessed by Short Questionnaire for Erectile Dysfunction (SQUED) Spanish version. The SQUED consist of 3 items. The 3 items are scored from 0 (severe dysfunction) to 15 (no dysfunction).
Assess adherence and satisfaction to treatment
It will be assessed by benefit, satisfaction and willingness to continue treatment questionnaire (BSD) Spanish version. The BSD consist of 3 items: perception of the benefit, satisfaction with the treatment and willingness of the patient to continue with the treatment. The 3 items are scored from 0 (no satisfaction and no adherence) to 10 (much satisfaction and adherence).

Secondary Outcome Measures

Full Information

First Posted
February 20, 2020
Last Updated
February 22, 2020
Sponsor
University of Alcala
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1. Study Identification

Unique Protocol Identification Number
NCT04284020
Brief Title
Educational Program Plus Physiotherapy After Prostatectomy
Official Title
Efficacy of Therapeutic Education After Radical Robotic Prostate Surgery: Randomized Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
February 2020
Overall Recruitment Status
Unknown status
Study Start Date
December 1, 2019 (Actual)
Primary Completion Date
December 31, 2022 (Anticipated)
Study Completion Date
December 31, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Alcala

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
Objective: to find out the effectiveness of therapeutic education program plus pelvic-perineal physical therapy in radical robotic prostatectomy men in terms of quality of life (QoL), urinary incontinence (UI), erectile dysfunction (ED) and muscle strength. Design: Randomized, controlled and single blinded clinical trial. Participants will be randomly assigned in two groups. Experimental group: training pelvic-perineal physical therapy plus lifestyle education. Control group: training in pelvic-perineal physical therapy only. In the 2 groups several physical therapy measurements will be undertaken: 1st before physical therapy treatment, 2nd, 3 th and 4th after 3, 6 and 12 months after initial measurement. Study subjects: Post radical robotic prostatectomy men, which have not been already treated with adjuvant treatment and pelvic-perineal physical therapy, and after reading, understanding and freely signing an informed consent form. Sample size: 84 subjects will be included (42 subjects per group). To have a statistical power of 90% to detect an average difference of 10 points between two groups in the change of quality of life according to the questionnaire validated in Spanish SF-12, assuming a standard deviation of the change of 20 points based on the study from Hou et al, establishing an alpha risk of 0.05, in a bilateral contrast and assuming a 10% of drops outs. Data analysis: Separate analyzes of each variable collected in the two groups will be carried out. For continuous variables, means, medians, standard deviations and quartiles will be calculated, depending on the assumption or not, respectively, of the assumption of their normality previously determined with the Shapiro Wilk test (S-W). Qualitative variables will be described with absolute and relative percentage frequencies. Effectiveness will be evaluated by comparing between the two groups of the change in outcome variables between measurements.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostate Cancer, Side Effects

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
two groups: 1 experimental and 1 control group
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
84 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Educational program & pelvic floor muscle training
Arm Type
Experimental
Arm Description
The educational strategy will consist of explaining a healthy lifestyle guide with videos, mobile apps and activities about the anatomy of the pelvic floor and the physiology of the pelvic organs. It will be recommended to avoid risk factors, such as gaining weight, high impact sports, constipation, smoking, or drinking too much caffeine and alcohol. They will also instruct in toilet habits. The pelvic floor muscle training (PFMT) protocol will be applied. Participants will perform exercises with anal biofeedback, perineal and erectile dysfunction electrotherapy protocol and surface electromyography. They will perform PFMT in supine position, sitting, standing and walking. The intervention will last 5 weeks, 2 sessions per week. Each session will last 30/40 minutes. If the patients have overactive bladder symptoms they will perform transcutaneous tibial nerve stimulation (TTNS) protocol. The intervention will last 5 weeks, 2 sessions per week. Each session will last 30 minutes.
Arm Title
PFMT group
Arm Type
Active Comparator
Arm Description
They will receive a basic behavioral educational strategy in the first session including pelvic anatomy and physiology, recommendations to avoid risk factors and toilet habits. The PFMT protocol will be applied. Participants will perform PFMT exercises with anal biofeedback, perineal and erectile dysfunction electrotherapy protocol and surface electromyography. They will perform PFMT in supine position, sitting, standing and walking. The intervention will last 5 weeks, 2 sessions per week. Each session will last 30/40 minutes. If the patients have overactive bladder symptoms they will perform transcutaneous tibial nerve stimulation (TTNS) protocol. The intervention will last 5 weeks, 2 sessions per week. Each session will last 30 minutes.
Intervention Type
Behavioral
Intervention Name(s)
Therapeutic educational program
Intervention Description
See arm/group descriptions
Intervention Type
Other
Intervention Name(s)
PFMT
Other Intervention Name(s)
Pelvic floor muscle training
Intervention Description
See arm/group descriptions
Intervention Type
Other
Intervention Name(s)
TTNS
Other Intervention Name(s)
Transcutaneous tibial nerve stimulation
Intervention Description
See arm/group descriptions
Primary Outcome Measure Information:
Title
Change in QoL
Description
It will be assessed by Short Form 12 (SF-12) Spanish version. The SF-12 consist in 12 items of 8 dimensions: 2 items about physical function, 1 item about social function, 2 items about physical role, 2 items about emotional role, 2 items about mental health, 1 item about vitality, 1 items about body pain, 1 item about general health. The 8 dimensions are scored from 0 (bad health) to 100 (optimal state of health).
Time Frame
4 measurements to evaluate: before physical therapy treatment, 3 months, 6 months and 12 months after initial measurement.
Title
Change in UI
Description
It will be assessed by International Consultation on Incontinence Questionnaire Urinary Incontinence (ICIQ-UI) Spanish version. The ICIQ-UI SF consist in 3 items (Frequency, Quantity and Impact) and 8 questions to identify the UI type. The 3 items are scored from 0 (no incontinence) to 21 (severe incontinence). It will be assessed by 1 hour Pad Test. The Pad test consists in weigh a compress after being used under standardized conditions.
Time Frame
4 measurements to evaluate: before physical therapy treatment, 3 months, 6 months and 12 months after initial measurement.
Title
Change in Prostatic Symptoms
Description
It will be assessed by International Prostate Symptom Score (IPSS) Spanish version. The IPSS consist of 6 items plus one about quality of life. The 6 items are scored from 1-7 (mild symptomatology), 8-19 (moderate symptomatology) to 20-35 (severe symptomatology).The item about quality of life is measured qualitatively.
Time Frame
4 measurements to evaluate: before physical therapy treatment, 3 months, 6 months and 12 months after initial measurement.
Title
Change in Pelvic Floor Muscle Strength
Description
The measuring consists of 4 factors: strength, relax, endurance and repeatability. It will be measured with manometry (mmHg).
Time Frame
4 measurements to evaluate: before physical therapy treatment, 3 months, 6 months and 12 months after initial measurement.
Title
Change in ED
Description
It will be assessed by Short Questionnaire for Erectile Dysfunction (SQUED) Spanish version. The SQUED consist of 3 items. The 3 items are scored from 0 (severe dysfunction) to 15 (no dysfunction).
Time Frame
4 measurements to evaluate: before physical therapy treatment, 3 months, 6 months and 12 months after initial measurement.
Title
Assess adherence and satisfaction to treatment
Description
It will be assessed by benefit, satisfaction and willingness to continue treatment questionnaire (BSD) Spanish version. The BSD consist of 3 items: perception of the benefit, satisfaction with the treatment and willingness of the patient to continue with the treatment. The 3 items are scored from 0 (no satisfaction and no adherence) to 10 (much satisfaction and adherence).
Time Frame
4 measurements to evaluate: before physical therapy treatment, 3 months, 6 months and 12 months after initial measurement.

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Men had undergone radical robotic prostate surgery. Men reading, understanding and freely signing an informed consent form. Exclusion Criteria: Participants who had received adjuvant therapies (chemotherapy, radiotherapy) before pelvic-perineal physical therapy treatment. Men with a history of pelvic organ surgery. Men with chronic diseases that affects their quality of life. Participants with psychiatric or neurological problems. Postoperative men with cognitive limitations to understand information, respond to questionnaires, consent and / or participate in the study.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Cristina Romojaro-Pérez, PhD student
Email
cromojaroperez@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Cristina Romojaro-Pérez, PhD student
Phone
915 75 96 51
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Maria Torres-Lacomba, PhD
Organizational Affiliation
University of Alcalá. FPSM research group. HUPA
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Beatriz Navarro-Brázalez, PhD
Organizational Affiliation
University of Alcalá. FPSM research group. HUPA
Official's Role
Study Chair
Facility Information:
Facility Name
University of Alcalá. FPSM research group. HUPA
City
Alcalá de Henares
State/Province
Madrid
ZIP/Postal Code
28805
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
María Torres-Lacomba, PhD
Email
maria.torres@uah.es
First Name & Middle Initial & Last Name & Degree
Cristina Romojaro-Pérez, PhD student
Email
cromojaroperez@gmail.com

12. IPD Sharing Statement

Plan to Share IPD
No

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Educational Program Plus Physiotherapy After Prostatectomy

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