- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04777461
Living With Polycystic Ovary Syndrome (LW-PCOS)
Living With Polycystic Ovary Syndrome- Structured Education Programme
Study Overview
Status
Conditions
Intervention / Treatment
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
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Hull, United Kingdom, HU32RW
- Hull University Teaching Hospitals NHS Trust, Academic diabetes, Endocrinology and metabolism
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
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.
Study Plan
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 |
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EXPERIMENTAL: Group 1
Pilot the structured education in women with PCOS
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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.
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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
Sponsor
Collaborators
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- LW-PCOS V1.2020
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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