Condition category
Urological and Genital Diseases
Date applied
Date assigned
Last edited
Retrospectively registered
Overall trial status
Recruitment status
No longer recruiting
Publication status

Plain English Summary

Background and study aims
Urinary incontinence (UI) is a distressing condition that limits people’s quality of life and places a heavy financial burden on health and social care services. Behavioural treatments are recommended as a first-line treatment worldwide. A multifaceted evidence-based self-management package was developed following the Medical Research Council (MRC) framework for developing and evaluating complex interventions. This study aims to evaluate the feasibility and acceptability and provide preliminary outcomes of the effectiveness of the intervention in older women living with UI.

Who can participate?
Women aged 55 or over living with a symptom of urine leakage who are able to read and speak the English Language will be eligible to take part. However, individuals suffering from UI caused by neurological diseases affecting the brain and spinal cord, or are cognitive impaired will be excluded.

What does the study involve?
A total of 50 women are randomly allocated to two groups: a 3-month course of self-management package with an opportunity to request a single support session, or a control group who receive the package at 3 months. Participants are asked to complete a set of questionnaires at baseline and 3-month follow-up. At 3 months a smaller number of participants who have been given the package are invited to have an individual interview talking about their experiences of using the package.

What are the possible benefits and risks of participating?
The information from this study is unlikely to benefit participants directly, but the researchers will share a summary of the results. Taking part will give participants the opportunity to practise some self-management skills and receive relevant information included in the package. It will also give the opportunity for their views and experiences to be heard and the information may help refine the self-management package, which may support older women with UI in the future. The researchers do not anticipate any risks. Participants may find talking about their experiences touches upon personal topics around incontinence and related issues. They do not have to answer any questions they do not wish to and they may pause or stop the interview at any time. The interviewer has a background in medicine and experience in dealing with distressed patients and will advise participants to see their general practitioner if necessary.

Where is the study run from?
University of Leeds (UK)

When is the study starting and how long is it expected to run for?
April 2016 to August 2019

Who is funding the study?
Leeds Benevolent Society for Single Ladies (LBSSL) (UK)

Who is the main contact?
Dr Yu Fu

Trial website

Contact information



Primary contact

Dr Yu Fu


Contact details

Worsley Building
Academic Unit of Palliative Care
Leeds Institute of Health Sciences
School of Medicine
University of Leeds
United Kingdom
+44 (0)113 3437351

Additional identifiers

EudraCT number

Nil known number

Nil known

Protocol/serial number

Nil known

Study information

Scientific title

An evidence-based self-management package for urinary incontinence in older women: a mixed methods feasibility study


Study hypothesis

Urinary incontinence (UI) is a distressing condition that limits people’s quality of life and places a heavy financial burden on health and social care services. Although several options are available for treating and managing UI, behavioural treatments are recommended as a first-line treatment worldwide.
A multifaceted intervention involving a trial of behavioural strategies has been considered to be more effective than a single component for the management of UI in older women. Self-management for chronic conditions is a multidimensional construct and defined as an intervention designed to develop individuals’ knowledge, skills or psychological and social resources and their ability to manage their health condition and consequences, through education, training and support. However, evidence for self-management programmes incorporating multifaceted behavioural treatments for use in UI among older women is currently limited.
An evidence-based self-management package has been co-developed with older women with UI and health professionals providing treatment and care. However, the feasibility and acceptability of using this package to self-manage women's UI remained unknown.

Ethics approval

Approved 09/10/2018, School of Healthcare Research Ethics Committee at the University of Leeds (The Secretariat, University of Leeds, Leeds, LS2 9JT, UK; Tel: +44 (0)113 3431642; Email:, ref: HREC 18-001

Study design

Mixed-methods approach comprising a two-arm RCT with a nested qualitative study

Primary study design


Secondary study design

Randomised controlled trial

Trial setting


Trial type


Patient information sheet

Not available in web format, please use contact details to request a participant information sheet


Urinary incontinence


Eligible women will be randomised using a 1:1 ratio to either the intervention or control group. The randomisation procedure will be performed by a web-based randomisation service (

The intervention group receive a 3-month course of self-management package with an opportunity to request a single support session
The control group do not receive the self-management package or the support session. However, they are informed that they will receive the package only at the end of this study (at three months).

The experimental intervention was the self-management package, co-developed with older women living with UI, health professionals and lay members. The aim of the package was to provide information and practical skills for women to self-manage their UI and other symptoms. Following elements were included: recognition and awareness, getting the support you need, understanding the cause, learning to manage your UI, developing a self-management plan and how can you find out more. Descriptions of self-management techniques such as PFME, bladder training and lifestyle interventions were also provided. The researcher with medical background acted as a facilitator and delivered the intervention in person straight after the completion of baseline data collection. A self-management brochure was also distributed. The intervention group were also informed that they could request a single one-hour support session with the researcher on how to use the package and/or addressing questions or concerns that they may have.

Both groups will be assessed at the start of the study and 3 months later. Measures will include generic and disease-specific quality of life, UI severity, self-efficacy and psychological health status. Some participants will be interviewed to facilitate the understanding of how the package might work and further explore facilitators and barriers to acceptance of the self-management package.

Findings will inform the design of the larger trial, provide information about the feasibility of offering self-management package to older women with UI, and produce preliminary outcomes about its effectiveness. Findings will be shared with women and professionals and with service commissioners.

Intervention type



Drug names

Primary outcome measure

1. Generic quality of life is measured using EQ-5D-5L at baseline and 3-month follow up
2. Disease-specific quality of life is measured using King’s Health Questionnaire at baseline and 3-month follow up
3. UI severity is measured using international consultation on incontinence questionnaire short form at baseline and 3-month follow up
4. Self-efficacy is measured using the geriatric self-efficacy index for urinary incontinence at baseline and 3-month follow up
5. Psychological health is measured using hospital anxiety and depression scale at baseline and 3-month follow up
6. Subjective improvement is measured using Global Impression: Improvement at 3-month follow up for the intervention group only

Secondary outcome measures

There are no secondary outcome measures

Overall trial start date


Overall trial end date


Reason abandoned (if study stopped)


Participant inclusion criteria

1. Women aged 55 or over
2. Self reported symptom of any involuntary leakage of urine
3. Be able to read and understand English

Participant type


Age group




Target number of participants

UK sample size: 50

Total final enrolment


Participant exclusion criteria

1. Aged under 55 years
2. No symptoms of urine leakage
3. UI caused by neurological diseases affecting the brain and spinal cord
4. Cognitive impaired

Recruitment start date


Recruitment end date



Countries of recruitment

United Kingdom

Trial participating centre

Leeds Older People's Forum
Suite C24 Joseph’s Well Hanover Walk Westgate
United Kingdom

Sponsor information


University of Leeds

Sponsor details

University of Leeds
Woodhouse Lane
United Kingdom
+44 (0)113 3431642

Sponsor type




Funder type


Funder name

Leeds Benevolent Society for Single Ladies (LBSSL)

Alternative name(s)

Funding Body Type

Funding Body Subtype


Results and Publications

Publication and dissemination plan

To be published by the end of 2019.

IPD sharing statement
The datasets generated during and/or analysed during the current study are not expected to be made available as the researchers are not allowed to share any research data with anyone outside the direct research team.

Intention to publish date


Participant level data

Not expected to be available

Basic results (scientific)

Publication list

2020 results in (added 18/06/2020)

Publication citations

Additional files

Editorial Notes

18/06/2020: Publication reference and total final enrolment number added. 04/09/2019: Trial's existence confirmed by ethics committee.