- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03241524
Consistency of Questionnaires to Evaluating Sexual Functions in Young Healthy Women
August 2, 2017 updated by: Christiane Kelen Lucena da Costa, Universidade Federal do Rio Grande do Norte
Consistency of Three Different Questionnaires to Evaluating Sexual Functions in Young Healthy Women Before and After a Pelvic Floor Muscle Training Program
The sample comprised 31 female undergraduate students attending a private University in João Pessoa, northeastern Brazil.
The inclusion criteria were: age between 19 and 35 years, heterosexual, active sex life, living in a stable relationship for at least 6 months no pregnancy or parturition in the last 6 months, clinically healthy and agreeing with the terms for participating in the study.
All participants gave their informed consent to take part in the study.
Study Overview
Status
Completed
Intervention / Treatment
Detailed Description
PURPOSE: To compare the consistency of 3 instruments for sexual function evaluation in healthy young women before and after a pelvic floor muscle training.
Methods: Thirty-one healthy young women were enrolled in an 8-week training program, consisting of bipedal exercises performed at home.
The PERFECT and Peritron methods were used to estimate the efficacy of the intervention on pelvic muscles.
Three questionnaires (FSFI, SQ-F and GRISS) were applied to assess sexual function.
Both procedures were performed on three occasions: before, 4 and 8 weeks after the start of the training program.
ANOVA for repeat measures and Tukey's post hoc were applied to analyze PERFECT and Peritron results, as well as individual domains and total scores of the questionnaires.
The accuracy measured by the area under the ROC curve (AUC) for individual domains of each questionnaire and cross-validated pairwise comparison of the three instruments were also analyzed.
Study Type
Interventional
Enrollment (Actual)
31
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
PB
-
Joao Pessoa, PB, Brazil, 58038-10
- Laboratory of Physical Therapy
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
19 years to 35 years (ADULT)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Female
Description
Inclusion Criteria:
- age between 19 and 35 years;
- heterosexual with active sex life, living in a stable relationship for at least 6 months;
- no pregnancy or parturition in the last 6 months;
- clinically healthy;
- agreeing with the terms for participating in the study;
- To sign and agree with their informed consent to take part in the study.
Exclusion Criteria:
- Do not continue with the intervention program.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: PREVENTION
- Allocation: NA
- Interventional Model: SINGLE_GROUP
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
EXPERIMENTAL: Exercise program for pelvic muscle floor
Training program for pelvic muscles and application of 3 questionnaires for sexual function evaluation and the use of PERFECT and Perina methods to evaluate perineal musculature.
|
Pelvic muscles of each participant was evaluated by PERFECT and Peritron methods in terms of strengthening as well as sexual function response using 3 questionnaires, before and after 4 and 8 weeks from the beggining of an exercise program prescribed according to individual ratings obtained in the previous evaluation.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Assessment of female sexual response by Female Sexual Function Inventory (FSFI)
Time Frame: 8 weeks
|
This questionnaire contains 19 itens assessing sexual function over the past four weeks, associated with six domains and possible types of disorders: desire, arousal, lubrification, orgasm, satisfaction of sexual life, and pain during or after the intercourse.
|
8 weeks
|
|
Assessment of female sexual response by Sexual quotient for women (QS-F)
Time Frame: 8 weeks
|
This instrument is composed of 10 questions that assess sexual function, adressing desire and interest in sex, foreplay, sexual arousal and harmony with the partner, comfort in sexual intercourse, and orgasm and sexual satisfaction.
The overall scores range from 0 to 100, where high scores mean excellent sexual performance.
|
8 weeks
|
|
Assessment of female sexual response by Golombok-Rust Inventory of Sexual Satisfaction (GRISS) for female.
Time Frame: 8 weeks
|
The GRISS is a 28-item questionnaire that provides a total GRISS score as well as two separate scales for males and females.
For females, the scale has 8 items, including anorgasmia, vaginismus, non-communication, infrequency, female avoidance, female non-sensuality, female dissatisfaction and anorgasmia.
Scoring was from 0 to 10 with values higher than 5 indicating sexual dysfunction.
|
8 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Pelvic floor muscles performance quantified by PERFECT method
Time Frame: 8 weeks
|
This method is an acronym for the evaluation of contractile components of the pelvic floor muscles and was validated with high test-retest reliability, producing significant correlations for the variables, in particular, power and endurance.
According to definitions of these methods, P indicates power or pressure, which corresponds to muscle strength estimated by manometry biofeedback or digital touch during voluntary maximum contraction.
The evaluation is based on Oxford modified scale: Degrees: 0 - no perineal contraction visible or by palpation (non-contraction); 1- no perineal contraction visible, recognized only by palpation; 2 - weak perineal contraction to palpation; 3 - perineal contraction present, but with nonresistance to palpation; 4 - perineal contraction present with counter-resistance to palpation of less than 5 seconds ; and 5 - perineal contraction present with counter-resistance to palpation of more than 5 seconds.
|
8 weeks
|
|
Pelvic floor muscles performance quantified by PERITRON method
Time Frame: 8 weeks
|
The Peritron is a hand-held clinical biofeedback perineometer used for assessing the strength of the pelvic floor muscles.
The device helps teach patients how to effectively perform pelvic floor exercises (kegels).
Pelvic floor contraction causes air pressure in the sensor to be transferred through the connecting tube and displayed on the readout unit.
|
8 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Sacomori C, Virtuoso JF, Kruger AP, Cardoso FL. [Pelvic floor muscle strength and sexual function in women]. Fisioterapia e Movimento, 28, 657-665, 2015.
- Damjanovic A, Duisin D, Barisic J. The evolution of the female sexual response concept: treatment implications. Srp Arh Celok Lek. 2013 Mar-Apr;141(3-4):268-74. doi: 10.2298/sarh1304268d.
- da Costa CKL, Spyrides MHC, de Sousa MBC. Consistency of three different questionnaires for evaluating sexual function in healthy young women. BMC Womens Health. 2018 Dec 20;18(1):204. doi: 10.1186/s12905-018-0693-y.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (ACTUAL)
March 12, 2016
Primary Completion (ACTUAL)
June 20, 2016
Study Completion (ACTUAL)
September 12, 2016
Study Registration Dates
First Submitted
March 29, 2017
First Submitted That Met QC Criteria
August 2, 2017
First Posted (ACTUAL)
August 7, 2017
Study Record Updates
Last Update Posted (ACTUAL)
August 7, 2017
Last Update Submitted That Met QC Criteria
August 2, 2017
Last Verified
August 1, 2017
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 28032017
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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