MENO_edu: Effectiveness of Assessment and Educational Intervention on Motor Control of the Pelvic Floor Muscle in Women

Sponsor
University of Malaga (Other)
Overall Status
Completed
CT.gov ID
NCT03220672
Collaborator
(none)
120
1
5.9

Study Details

Study Description

Brief Summary

The goal of the present study is to evaluate the short and long term effectiveness of a tailored assessment and educational intervention on motor control of the pelvic floor muscle in menopausal and non-menopausal women.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Tailored assessment and educational
N/A

Detailed Description

Menopausal transition has been related to stress urinary incontinence. The transition from the reproductive to the non-reproductive period is induced by a decrease in sex hormone production in the ovaries. Climacteric-stage oestrogen deficiency produces genital and urinary tract atrophy, which may be related to symptoms such as urinary frequency, urinary urgency, nocturia incontinence, and recurrent urinary tract infection. Urinary incontinence seems to appear due to a combination of factors such as pelvic floor weakness and tearing, denervation and fascial tears as well as both loss of motor units and altered activation patterns. However, physiotherapy can treat weakness and altered motor control in order to compensate for other factors. In fact, physiotherapy is considered the treatment of first choice.

Besides evidence defending physiotherapy as first line conservative therapy in incontinence due to influence of strength and motor control in this pathology and its prevalence in perimenopause women, little is known about its effects in this population. Hence, the aim of this study is to evaluate the short and long term effectiveness of a tailored assessment and educational intervention on motor control of the pelvic floor muscle in menopausal and peri-menopausal women.

Study Design

Study Type:
Interventional
Actual Enrollment :
120 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Effectiveness of a Tailored Assessment and Educational Intervention on Motor Control of the Pelvic Floor Muscle in Menopausal and Peri-menopausal Women
Actual Study Start Date :
Jan 1, 2017
Actual Primary Completion Date :
Jun 1, 2017
Actual Study Completion Date :
Jul 1, 2017

Arms and Interventions

Arm Intervention/Treatment
Experimental: Expertimental

The sample will receive a tailored assessment and educational intervention on Motor Control of the Pelvic Floor Muscle

Behavioral: Tailored assessment and educational
Intervention will consist of 45 minutes of anatomy education, pelvic floor assessment and neuromuscular re-education. Women will be given an explanation of how the pelvis is composed, including the viscera and pelvic floor function and anatomy, through a simple explanatory sheet. They will be also informed of the causes of pelvic floor deterioration as well as its consequences.. Neuromuscular re-education will continued by teaching them how to perform slow contractions, fast contractions and lifting contraction. They will be also shown vaginal cones and advised on possible treatment methods if they were needed. After that, women will be given a tip sheet to improve pelvic floor function. Those recommendations will included: Tips to take into account during habits like urination, doing sport, gymnastics or any efforts, pelvic floor muscles exercises and how to use vaginal cones adequately.

Outcome Measures

Primary Outcome Measures

  1. Motor Control of Pelvic Floor Muscle by single questionnare [inmediate effect post education]

    Women will report an outcome regarding tightening capacity after intervention. It consisted of a one item questionnaire about pelvic floor contraction capacity. It is chosen by the expert panel developed by researcher from this project. The item is a question regarding tightening capacity and it had a polychotomous answer: "How is the tightening capacity of your pelvic floor muscles? a) very high, b) high, c) good, d) optimal, e) bad, f) low, g) very low"

Secondary Outcome Measures

  1. Anthropometric [baseline, inmediate effect post education and 2,4 and 12 weeks. Long time effect 6 months]

    Age, height and weight, and their Body Mass Index (BMI) was calculated.

  2. Interview about urinary incontinence [baseline, inmediate effect post education and 2,4 and 12 weeks. Long time effect 6 months]

    Women will also underwent an interview about urinary incontinence with a physiotherapist from the Consulting Unit of Physiotherapy of the Pelvic Floor. The questionnaire consisted of 38 items regarding delivery conditions, faecal and urinary incontinence as well as medical conditions and lifestyle. This interview includes information from descriptive outcomes reported by the clinician, so pelvic floor muscles will be evaluated by both manual muscle testing and a perineometer. Hence, this interview has both qualitative and quantitative reponses.

  3. The International Consultation on Incontinence Questionnaire (ICIQ-UI SHORT FORM) [baseline, inmediate effect post education and 2,4 and 12 weeks. Long time effect 6 months]

    The ICIQ is a simple and short questionnaire to assess the symptoms and impact of UI across the population. It consists of 3 items which indicate frequency, quantity and impact, and 8 questions more related to the symptoms indicative of the type of UI, but not being contemplated when obtaining a global index. The ICIQ-UI short form has a good reliability with a Cronbach's alpha of 0.95. It was validated in Spanish by Espuña et al, with a Cronbach's alpha of 0.89

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • All participants in this study will sign an informed consent form prior their inclusion, and that whose participation will be voluntary
Exclusion Criteria:
  • Participants will be excluded if they have any cognitive disability, physical disability or psychiatric limitations that could limit the participation on the study test

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • University of Malaga

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Dr. Antonio I Cuesta-Vargas, Principal Researcher of CTS631 University of Malaga, University of Malaga
ClinicalTrials.gov Identifier:
NCT03220672
Other Study ID Numbers:
  • Meno_Edu_2017
First Posted:
Jul 18, 2017
Last Update Posted:
Jul 18, 2017
Last Verified:
Jun 1, 2017
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Dr. Antonio I Cuesta-Vargas, Principal Researcher of CTS631 University of Malaga, University of Malaga

Study Results

No Results Posted as of Jul 18, 2017