Living With Polycystic Ovary Syndrome (LW-PCOS)

November 21, 2021 updated by: Thozhukat Sathyapalan, University of Hull

Living With Polycystic Ovary Syndrome- Structured Education Programme

This project aims to develop and pilot an evidence-based structured education program that can be run in groups to enable women with PCOS to make lifestyle changes, which will help them improve their PCOS and reduce the risk of future PCOS-related complications.

Study Overview

Detailed Description

The first aim of this project is to develop an evidence-based structured education programme for women with PCOS. According to the Medical Research Council framework for complex interventions, robust patient-education programmes should have an evidence-based structured written curriculum, which is delivered by trained educators and is regularly assessed and audited. To meet these standards, the investigators first aim to develop a written curriculum for the structured education programme, written presentation material for the educational sessions and participants' handouts, but also material for training for the educators who will deliver the programme.

The philosophy of the programme is based on patient empowerment. The structured group education programme will be based on psychological theories of learning including the Leventhal's common-sense theory, the dual-process theory, and the social learning theory. Similar to previous successful programmes in diabetes education and based on the experience gained by conducting the education programme "Living with type 2 diabetes" in our centre, the programme will be designed as a six-hour of education programme with a formal and informed curriculum. It will be offered in two three-hour sessions of teaching for 8-12 PCOS women at a time. Attendees will be encouraged to be accompanied by a person of their choice.

Initial thoughts on the curriculum and the format of the written material have been already discussed within our clinical and research team (Dr Papageorgiou, Professor Sathyapalan, Mrs Baldwin consultant endocrinologists, general practitioners and dietitian specialists/educators delivering the "Living with Diabetes" education programme for patients with type 2 diabetes) based on their experience and views expressed to them by women with PCOS. As such, the areas that will be covered in the structured education programme include:

  • Thoughts and feelings of the participants around PCOS
  • Understanding PCOS pathophysiology: what happens in the body
  • Understanding the risk factors (e.g., obesity) and health risks associated with PCOS
  • Emotional wellbeing and PCOS
  • Management of PCOS symptoms -how to take control:

    • Pharmacological options (i.e., hormonal contraceptives, anti-androgens, and insulin sensitisers)
    • Lifestyle changes (i.e., basics of energy balance, healthy eating based on Eat well Plate, mindful eating, physical activity recommendations, practical advice).
  • Planning for the future (e.g., family planning, screening for long-term conditions).

Importantly, the investigators are also going to conduct a patients' survey to find out what women with PCOS expect to gain from an educational programme addressing several aspects of PCOS. The investigators will use the collected data to further refine the aspects of PCOS that will be included in the final curriculum of the programme.

Study Type

Interventional

Enrollment (Actual)

30

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

      • Hull, United Kingdom, HU32RW
        • Hull University Teaching Hospitals NHS Trust, Academic diabetes, Endocrinology and metabolism

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

18 years to 50 years (ADULT)

Accepts Healthy Volunteers

No

Genders Eligible for Study

Female

Description

Inclusion Criteria:

  1. Willingness and ability to provide signed informed consent before any study activity.
  2. Women aged 18-50 years (inclusive), with a confirmed diagnosis of PCOS based on Rotterdam criteria.
  3. Body mass index > 25 kg/m²

Exclusion Criteria:

  1. Participants under 18 years or over 50 years old.
  2. Participants who cannot adequately understand verbal and written explanations given in English.
  3. Lack of mental capacity to give written consent.

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: OTHER
  • Allocation: NA
  • Interventional Model: SINGLE_GROUP
  • Masking: NONE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: Group 1
Pilot the structured education in women with PCOS
The outcome of this survey will help with developing curriculum for the structured education programme.
The questionnaire is aimed to capture the knowledge and expectations of the participants from taking part in the educational sessions.
Piloting the education program through 2 educational group sessions
The questionnaire aimed to capture participant's satisfactions and knowledge gained by taking part in the pilot study
This aimed to capture skills developed, knowledge gained and changes in participants behaviour and perceptions by taking part in the pilot study.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
develop an evidence-based structured education programme for women with PCOS
Time Frame: 12 months

Conducting a survey among women with PCOS to understand the service user's perspectives on the development of an educational programme for PCOS.

The survey measures the need and knowledge about PCOS. The scales measures form 1 to 5. In which 1 is minimum or 5 is maximum. for example

Information about PCOS

1. Do you think you have enough knowledge about PCOS? Please circle the answer in the scale below

1 2 3 4 5

12 months
Pilot the structured education programme
Time Frame: 12 months

cognitive outcomes related to PCOS, monitor and evaluate the education process

the post-pilot survey measures the satisfaction about the education session, the knowledge gained and the skills developed from the education session, the cognitive outcome and illness perception on a scale of 1 to 5 where 1 is minimum and 5 is maximum. for example

How often do you think about your illness?

1 2 3 4 5

12 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

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)

September 1, 2021

Primary Completion (ACTUAL)

October 31, 2021

Study Completion (ACTUAL)

October 31, 2021

Study Registration Dates

First Submitted

September 26, 2020

First Submitted That Met QC Criteria

February 25, 2021

First Posted (ACTUAL)

March 2, 2021

Study Record Updates

Last Update Posted (ACTUAL)

November 23, 2021

Last Update Submitted That Met QC Criteria

November 21, 2021

Last Verified

November 1, 2021

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

There is no plan to make any identifiable participants data available to anyone. the final results will be published in one of the medical journals

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

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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