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CompletedNCT02614105UriCOUpdated Mar 3, 2021

Urinary Incontinence Amongst Women With Chronic Obstructive Pulmonary Disease

An interventional study of Pelvic floor muscle training and Cough-suppression therapy in Chronic Obstructive Pulmonary Disease and Urinary Incontinence, sponsored by Ostfold Hospital Trust. Completed at 2 sites in Norway. Open to female participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2021-03-03.

Sponsored by Ostfold Hospital Trust · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
35
Allocation
Randomized
Ages
18 Years and older
Sex
Female
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Study summary

The primary aim of the study is to investigate whether pelvic floor muscle training or cough-suppression therapy reduces symptoms of urinary incontinence amongst women with chronic obstructive pulmonary disease grade 1-4 (mild to very severe disease).

Read the detailed description

This two-centre study will consist of a randomised controlled trial (RCT) with a parallel group design and include two intervention groups and one control group. Recruitment and data collection will occur simultaneously at the ØHT and St. Olav's Hospital in Trondheim.

All participants will complete an initial four week general group exercise class (1 hour once a week) prior to randomisation. This intervention will focus on strength exercises (lower limb and upper limb), endurance training, balance training and thorax mobilising exercises. All participants will be examined and complete questionnaires at two occasions; after the initial four weeks general exercise/before intervention, and at 16 weeks post-randomisation.

Participants will be randomised to either Intervention group A (pelvic floor muscle training group), Intervention group B (cough-suppression group) or a control group who will receive brief written information about pelvic floor muscle training and cough-suppression, but no other form of regular follow-up or intervention throughout the intervention period.

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Conditions studied

03

In context

Lung Diseases

3,303 studies on the registry are indexed under Lung Diseases; 355 are open to participants now.

This study's enrollment of 35 is below the median of 72 across 2,118 interventional studies indexed under Lung Diseases.

Browse Lung Diseases studies →

Lead sponsor

Ostfold Hospital Trust is the lead sponsor of 48 studies on the registry; 10 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
Female
Accepts healthy volunteers
No

Inclusion criteria

  • COPD grade 1-4
  • Subjective urinary incontinence
  • Ability to perform an active contraction of the pelvic floor muscles

Exclusion criteria

Exclusion Criteria:

  • Unstable COPD
  • More than 4 hospital admissions due to COPD in the past twelve months
  • Neurological conditions
  • Previous gynecological surgery
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Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
35 participants (actual)

Study arms

  • Experimental
    Pelvic floor muscle training

    Participants in the pelvic floor muscle training group will receive group exercise sessions (1 hour) at the physiotherapy out-patient department of the hospital once a week for 16 weeks with guidance from an experienced pelvic floor physiotherapist. The group exercise sessions will focus on pelvic floor muscle training, relaxation and breathing techniques. Participants in the pelvic floor muscle training group will also receive an individually adapted pelvic floor muscle training program for daily home use.

    Procedure: Pelvic floor muscle training

  • Experimental
    Cough-suppression

    Participants in the cough-suppression group will receive a group education session with general information about cough-suppression therapy and advice about how to distinguish between unproductive and productive cough to enable them to perform airway clearance techniques when required. In addition, participants will receive one to two individual sessions (30-60 minutes) of cough-suppression therapy tailored to the individual needs based on symptoms and underlying disease activity

    Procedure: Cough-suppression therapy

  • Experimental
    Control group

    Participants in the group will receive guidance and instruction in terms of correct contraction of the pelvic floor muscles at clinical assessment. Control group participants will receive brief written information about pelvic floor muscle training and cough-suppression therapy, but no other form of regular follow-up or intervention throughout the intervention period.

    Other: Control

Interventions

  • ProcedurePelvic floor muscle training

    16 weeks of group-based exercise

  • ProcedureCough-suppression therapy

    Group and individual sessions of respiratory physiotherapy with focus on techniques to suppress cough

  • OtherControl

    Brief information only

06

What researchers measure

Primary outcomes

  1. International Consultation on Incontinence Questionnaire Short form (ICIQ_SF)

    Participants in the group will receive guidance and instruction in terms of correct contraction of the pelvic floor muscles at clinical assessment. Control group participants will receive brief written information about pelvic floor muscle training and cough-suppression therapy, but no other form of regular follow-up or intervention throughout the intervention period.

    Time frame: Change from baseline score at 16 weeks

Secondary outcomes

  1. Cough symptoms

    Cough symptoms will be measured using the Norwegian version of the Leicester Cough Questionnaire, which is in the process of being translated from English to Norwegian and tested for reliability and validity. The Leicester Cough Questionnaire is used to measure physical, psychological and social factors related to cough

    Time frame: Change from baseline score at 16 weeks

  2. Chronic Obstructive Pulmonary Disease symptoms

    A subjective evaluation of their Chronic Obstructive Pulmonary Disease symptoms (including cough) using the COPD Assessment Test (CAT). CAT is a disease-specific questionnaire which measures subjective symptoms of Chronic Obstructive Pulmonary Disease.

    Time frame: Change from baseline score at 16 weeks

  3. Self-reported function and quality of life

    COOP/WONCA is quick and easy to complete and has demonstrated good validity and reliability both in Norwegian and in the Chronic Obstructive Pulmonary Disease population

    Time frame: Change from baseline score at 16 weeks

  4. Voluntary pelvic floor muscle function

    Voluntary pelvic floor muscle function will be evaluated using digital palpation and scored on a 1-4 scale according to the International Continence Society Score.

    Time frame: Change from baseline score at 16 weeks

  5. Pelvic floor muscle strength

    Pelvic floor muscle strength will be measured using Peritron.

    Time frame: Change from baseline score at 16 weeks

  6. Field walking test

    Participants will also perform the six-minute walk test at inclusion and after the intervention to explore whether the intervention results in a change in general physical capacity.

    Time frame: Change from baseline score at 16 weeks

  7. Physical activity

    Physical activity will be measured using an activity monitor (pedometer) which the participants will wear throughout the whole intervention period to investigate whether a change in urinary incontinence affects physical activity

    Time frame: Change from baseline score at 16 weeks

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Study locations

2 sites
  • St Olavs Hospital
    Trondheim, Norway
  • Østfold Hospital Trust
    Moss, Østfold, Norway
08

References and documents

Publications

  • Haukeland-Parker S, Frisk B, Spruit MA, Stafne SN, Johannessen HH. Treatment of urinary incontinence in women with chronic obstructive pulmonary disease-a randomised controlled study. Trials. 2021 Dec 11;22(1):900. doi: 10.1186/s13063-021-05816-2. PubMed 34895285 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 3, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02614105
Lead sponsor
Ostfold Hospital Trust
Collaborators
St. Olavs Hospital
Responsible party
Stacey Haukeland Parker (MSc/senior physiotherapist, Ostfold Hospital Trust) — Principal investigator
First posted
Nov 25, 2015
Start date
Nov 2015
Primary completion
Dec 2018
Completion
Dec 2018
Last update
Mar 3, 2021

Study contacts

Hege Hølmo Johannessen, PhD
principal investigator · Ostfold Hospital

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Mar 2021. You cannot join it, but the record below documents what was studied.

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