NCT04009694

Brief Summary

The trial design is a quasi-experimental cohort trial that includes women referred for pelvic organ prolapse specific physiotherapy. Candidates will be selected via a convenience sampling method from four physiotherapy outpatient departments at a NHS trust within Greater Manchester. The data collection occurred in January-June 2019 and ethical approval was granted by School Research Ethics, University of Salford. Treatment aims to ensure there is respect for their autonomy, treatment is fair (Justice), no harm is done to the participant (nonmaleficence) and treatment benefits the participants (beneficence). Participants are required to complete a consent form prior to their initial session. To ensure methodological quality, the STROBE guidelines will be followed to make certain all apt information required is reported to allow for replication of the intervention. The trial aims to include (n=60) women with a diagnosed pelvic organ prolapse. They are required to complete 16 weeks of supervised pelvic floor exercises with a specialist physiotherapist as documented within the most recent NICE guidelines. The outcome measures used will be the Pelvic Organ Prolapse symptom score (POPSS) and this will be documented before and after the 16 week period. Along side the POPSS, the patients body mass index and severity of pelvic organ prolapse will also be recorded and the results of this will be correlated post trial using the relevant data analysis testing methods.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
60

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Sep 2018

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

September 1, 2018

Completed
10 months until next milestone

First Submitted

Initial submission to the registry

July 2, 2019

Completed
3 days until next milestone

First Posted

Study publicly available on registry

July 5, 2019

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2019

Completed
9 days until next milestone

Study Completion

Last participant's last visit for all outcomes

September 10, 2019

Completed
Last Updated

July 9, 2019

Status Verified

July 1, 2019

Enrollment Period

1 year

First QC Date

July 2, 2019

Last Update Submit

July 5, 2019

Conditions

Keywords

Pelvic floor muscle trainingpelvic physiotherapypelvic floor exercises

Outcome Measures

Primary Outcomes (1)

  • Pelvic Organ Prolapse Symptom Score (POPSS)

    The POPSS is a patient-reported Outcome Measure consisting of seven POP symptom specific items, each with a five-point Likert response set (0 = never, 1 = occasionally, 2 = sometimes, 3 = most of the time and 4 = all of the time). The minimum score is 0 which would indicate that the pelvic organ prolapse in a-symptomatic and the maximum score for the POPSS is 28 which would indicate higher severity in pelvic organ prolapse symptoms. In addition, the women select a specific symptom which is most bothersome for them.

    sixteen weeks

Study Arms (1)

Pelvic Floor Muscle Training

EXPERIMENTAL

Sixteen weeks of supervised pelvic floor muscle training with a specialist physiotherapist. Participants will be assessed at weeks 0 / 4 / 10 \& 16 and the outcome measures will be recorded at week 0 \& week 16. During each assessment, participants will be educated regarding the anatomy of pelvic organ prolapses and the pelvic floor muscles. They will be taught how to contract their pelvic floor, offered a vaginal examination, given a personalised pelvic floor muscle training programme (including the Knack) - up to a ten second hold long contractions (x 10 repitations) and up to 10 quick contractions. They will also be taught a sub max contraction for up to 30 seconds, offered lifestyle management advice including avoiding heavy lifting or straining. A leaflet explaining the aforementioned information will also be provided at the initial assessment.

Other: Pelvic Floor Muscle training

Interventions

Sixteen weeks of supervised pelvic floor muscle training with a specialist physiotherapist

Pelvic Floor Muscle Training

Eligibility Criteria

Age18 Years+
Sexfemale(Gender-based eligibility)
Gender Eligibility DetailsPelvic organ prolapse is a condition exclusive to women
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Gynaecologist diagnosed women with a mild / moderate or severe pelvic organ prolapse
  • \>18 years old

You may not qualify if:

  • Unwilling or unable to provide informed consent (opt out of treatment)
  • Unable to contract the pelvic floor muscles (determined by the treating physiotherapist)
  • History of Pelvic cancer / or radiotherapy treatment within three months,
  • Neurological or psychiatric disorders,
  • Untreated urinary tract infections,
  • Pregnant or planning to become pregnant or given birth within the past year,
  • Recent vaginal surgery within twelve weeks or evidence of genital oedema,
  • Suspected infection or fragility of the genital area As indicated by the referral source or patient reported at the initial assessment.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

National Health Service

Manchester, M8 5RB, United Kingdom

RECRUITING

MeSH Terms

Conditions

Pelvic Organ ProlapseUterine ProlapseProlapseCystoceleRectocele

Condition Hierarchy (Ancestors)

Pathological Conditions, AnatomicalPathological Conditions, Signs and SymptomsUterine DiseasesGenital Diseases, FemaleFemale Urogenital DiseasesFemale Urogenital Diseases and Pregnancy ComplicationsUrogenital DiseasesGenital DiseasesUrinary Bladder DiseasesUrologic DiseasesMale Urogenital DiseasesRectal DiseasesIntestinal DiseasesGastrointestinal DiseasesDigestive System DiseasesHernia

Study Officials

  • Nicky Spence, PhD

    University of Salford

    STUDY CHAIR

Central Study Contacts

Rebecca C Whittle, MSc

CONTACT

Nicky Spence, PhD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Rebecca Whittle BSc Hons. Specialist Pelvic Health Physiotherapist

Study Record Dates

First Submitted

July 2, 2019

First Posted

July 5, 2019

Study Start

September 1, 2018

Primary Completion

September 1, 2019

Study Completion

September 10, 2019

Last Updated

July 9, 2019

Record last verified: 2019-07

Data Sharing

IPD Sharing
Will share

Locations