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Living With Polycystic Ovary Syndrome (LW-PCOS)

Primary Purpose

Polycystic Ovary Syndrome

Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Survey on patient's perspectives on the development of an structured education programme for PCOS
Pre-pilot questionnaire
Piloting the structured education programme for PCOS
Post-pilot questionnaire
cognitive outcomes outcome evaluation form
Sponsored by
University of Hull
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Polycystic Ovary Syndrome

Eligibility Criteria

18 Years - 50 Years (Adult)FemaleDoes not accept healthy volunteers

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.

Sites / Locations

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

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Group 1

Arm Description

Pilot the structured education in women with PCOS

Outcomes

Primary Outcome Measures

develop an evidence-based structured education programme for women with PCOS
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
Pilot the structured education programme
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

Secondary Outcome Measures

Full Information

First Posted
September 26, 2020
Last Updated
November 21, 2021
Sponsor
University of Hull
Collaborators
British Dietetic Association
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1. Study Identification

Unique Protocol Identification Number
NCT04777461
Brief Title
Living With Polycystic Ovary Syndrome
Acronym
LW-PCOS
Official Title
Living With Polycystic Ovary Syndrome- Structured Education Programme
Study Type
Interventional

2. Study Status

Record Verification Date
November 2021
Overall Recruitment Status
Completed
Study Start Date
September 1, 2021 (Actual)
Primary Completion Date
October 31, 2021 (Actual)
Study Completion Date
October 31, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Hull
Collaborators
British Dietetic Association

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
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.
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Polycystic Ovary Syndrome

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
30 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Group 1
Arm Type
Experimental
Arm Description
Pilot the structured education in women with PCOS
Intervention Type
Other
Intervention Name(s)
Survey on patient's perspectives on the development of an structured education programme for PCOS
Intervention Description
The outcome of this survey will help with developing curriculum for the structured education programme.
Intervention Type
Other
Intervention Name(s)
Pre-pilot questionnaire
Intervention Description
The questionnaire is aimed to capture the knowledge and expectations of the participants from taking part in the educational sessions.
Intervention Type
Other
Intervention Name(s)
Piloting the structured education programme for PCOS
Intervention Description
Piloting the education program through 2 educational group sessions
Intervention Type
Other
Intervention Name(s)
Post-pilot questionnaire
Intervention Description
The questionnaire aimed to capture participant's satisfactions and knowledge gained by taking part in the pilot study
Intervention Type
Other
Intervention Name(s)
cognitive outcomes outcome evaluation form
Intervention Description
This aimed to capture skills developed, knowledge gained and changes in participants behaviour and perceptions by taking part in the pilot study.
Primary Outcome Measure Information:
Title
develop an evidence-based structured education programme for women with PCOS
Description
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
Time Frame
12 months
Title
Pilot the structured education programme
Description
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
Time Frame
12 months

10. Eligibility

Sex
Female
Gender Based
Yes
Gender Eligibility Description
Only female with PCOS aged between 18-50 years old will be involved
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Willingness and ability to provide signed informed consent before any study activity. Women aged 18-50 years (inclusive), with a confirmed diagnosis of PCOS based on Rotterdam criteria. Body mass index > 25 kg/m² Exclusion Criteria: Participants under 18 years or over 50 years old. Participants who cannot adequately understand verbal and written explanations given in English. Lack of mental capacity to give written consent.
Facility Information:
Facility Name
Hull University Teaching Hospitals NHS Trust, Academic diabetes, Endocrinology and metabolism
City
Hull
ZIP/Postal Code
HU32RW
Country
United Kingdom

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing 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

Learn more about this trial

Living With Polycystic Ovary Syndrome

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