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Diabetes Screening & Prevention for People With Learning (Intellectual) Disabilities:STOP Diabetes Study

2016年1月20日 更新者:University of Leicester

Screening for Glucose Intolerance and Development of a Lifestyle Education Programme for Prevention of Type 2 Diabetes in a Population With Learning Disabilities

People with learning (intellectual) disabilities have more health problems than the rest of the population; they are less likely to access help and have lifestyles that may increase their risk of getting diabetes (for example, poor diet and lack of physical activity). People with learning disabilities may also be prescribed drugs or have certain medical conditions (such as Down's syndrome) which can make their chances of getting diabetes greater.

Diabetes is a long-term condition, which can cause damage to the eyes, heart, kidneys, nerves and feet. Impaired glucose regulation happens when sugar levels in the blood are higher than normal but are not high enough to be diagnosed with diabetes. People with impaired glucose regulation are more likely to develop diabetes, heart disease and stroke in the future. If people with impaired glucose regulation make changes to their lifestyle (diet and exercise) they can prevent or delay getting diabetes.

The aim of this study is to screen people with learning disabilities for diabetes and impaired glucose regulation. The investigators also want to find out the best way to give people with learning disabilities some education around healthy lifestyles (for example, eating and exercise) to help with prevention of diabetes and cardiovascular disease. Therefore, the investigators also aim to develop a lifestyle education programme that is suitable for use in this population and test whether it is feasible and acceptable.

調査の概要

詳細な説明

Background -Adults with learning (intellectual) disabilities tend to have more health problems than the general population and are less likely to access help. Additionally, evidence suggests that due to a combination of lifestyle factors (e.g. poor diet, lack of physical activity), associated medical problems, and certain types of prescribed medication, people with learning disabilities may be at increased risk of developing type 2 diabetes and cardiovascular disease. Our overall aim is to undertake a programme of research that improves our knowledge and understanding of screening for impaired glucose regulation and type 2 diabetes in a population with learning disabilities, and to develop a lifestyle education programme for prevention of type 2 diabetes that is suitable for use in this population.

SCREENING PROGRAMME

Aim - The main programme of work consists of a large diabetes screening programme. The primary aim of the screening study is to evaluate the feasibility and clinical and cost effectiveness of a screening programme for identifying undiagnosed type 2 diabetes and impaired glucose regulation that is suitable for use in a population with learning disabilities.

Methods - A variety of approaches will be used to recruit people to the screening study: General practices will be approached first for participation in this study. If the practice does not agree, then the investigators will seek to approach eligible people on the Leicestershire Learning Disabilities Register. Learning disabilities consultants will also approach people face to face when attending for outpatient clinic appointments. Additionally, if individuals with learning disabilities (and/or their carer) contact the STOP Diabetes team to express an interest in the study, they will be given an invitation.

  • Volunteers will be asked to attend an appointment(s) where consent will be obtained and biomedical and demographic data collected. The consent process and data collection will be staged and people may need to attend between one to three appointments to complete.
  • People who are found to have type 2 diabetes or impaired glucose regulation will be asked to see their GP for care.
  • At every stage, reasonable adjustments will be made to take into account people's communication needs and decision making capacity. This may include involving a carer or a

DEVELOPMENT AND TESTING OF A STRUCTURED EDUCATION PROGRAMME

The aims of additional work being carried out alongside the screening study are to: (1) develop a lifestyle education programme to meet the needs of a population with learning disabilities and impaired glucose regulation or high risk of diabetes; (2) assess the feasibility of collecting outcome measures for participants with learning disabilities before and 3-months after they attend the education programme.

Methods - People approached to take part will be people who took part in the screening study and (1) gave their consent to be approached to take part in further phases of the research programme, and (2) were found to be at increased risk of developing diabetes according to their screening results.

Qualitative Interviews to inform curriculum development:

  • Interviews will be conducted with a sample of people with mild/moderate learning disabilities, their carers and healthcare professionals. Findings from the interviews will help inform development of an initial curriculum and education program.

Delivery of initial curriculum and obtaining feedback:

  • As part of the development work the education programme will be piloted with at least two groups of 6 - 8 people plus carers. Feedback will be collected from some of the people who attend the education sessions and any necessary changes made to the curriculum. These cycles of piloting, collecting feedback and modifying the programme will be repeated until the education programme developed is "fit for purpose".

Delivery of programme with collection of before and after measures:

  • Following initial development, testing and refinement of the curriculum, the education programme will be delivered with another sample of participants and the feasibility of collecting pre and post intervention outcome measures will be tested. The investigators anticipate delivering the programme to up to two groups of 6 - 8 people plus carers. Data will be collected at baseline and 3-months (12 weeks) following delivery of the final education session. Data and may include: physical activity and sedentary behaviour (as measured by accelerometer); body weight, BMI, waist circumference, blood pressure and dietary intake (fruit and vegetables). Uptake of the education programme (attendance) and retention at 3-months follow-up will also be explored. This phase will be subject to modification depending on the findings from prior iterations and any problems encountered.

研究の種類

観察的

入学 (実際)

930

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究場所

      • Leicester、イギリス、LE5 4PW
        • Diabetes Research Centre, University of Leicester

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

18年~74年 (大人、高齢者)

健康ボランティアの受け入れ

はい

受講資格のある性別

全て

サンプリング方法

非確率サンプル

調査対象母集団

Adults with a learning (intellectual) disability who are live in Leicester, Leicestershire or Rutland, UK;

説明

Inclusion Criteria:

  • Volunteer has a confirmed learning disability (permanent intellectual impairment);
  • Registered with a general practice in Leicester, Leicestershire or Rutland, UK;
  • Participant and/or carer has sufficient English language skills to enable fully informed consent to be obtained.

Exclusion Criteria:

  • Confirmed diagnosis of Type 2 diabetes or Type 1 Diabetes;
  • Malignancy or terminal illness;
  • Pregnancy or breast feeding;
  • Severe systemic disease that may interfere with measurement and interpretation of HbA1c.

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Glycosylated haemoglobin (HbA1c)
時間枠:Baseline screening appointment
Identification of type 2 diabetes, impaired glucose regulation, or normal glucose regulation
Baseline screening appointment
Plasma glucose
時間枠:Baseline screening appointment
Identification of type 2 diabetes, impaired glucose regulation, or normal glucose regulation
Baseline screening appointment

二次結果の測定

結果測定
メジャーの説明
時間枠
Physical activity levels (including sedentary behaviour)
時間枠:Baseline screening appointment
measured by accelerometer - only for a small sub-group
Baseline screening appointment
Obesity levels
時間枠:Baseline screening appointment
body mass index and waist size
Baseline screening appointment
Blood pressure
時間枠:Baseline screening appointment
systolic and diastolic
Baseline screening appointment
Lipids levels
時間枠:Baseline screening appointment
total cholesterol, LDL, HDL, triglycerides
Baseline screening appointment
Dietary/nutritional intake
時間枠:Baseline screening appointment
food groups and fruit and vegetable intake
Baseline screening appointment
Cardiovascular risk
時間枠:Baseline screening appointment
Framingham risk score
Baseline screening appointment
Health related quality of life
時間枠:Baseline screening appointment
EQ-5D
Baseline screening appointment
Behavioural disorders
時間枠:Baseline screening appointment
Aberrant Behaviour Checklist
Baseline screening appointment
Psychiatric disorders
時間枠:Baseline screening appointment
PAS-ADD checklist
Baseline screening appointment
Depression
時間枠:Baseline screening appointment
Glasgow Depression Scale and Carer Supplement
Baseline screening appointment

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

スポンサー

捜査官

  • 主任研究者:Prof Kamlesh Khunti, PhD, FRCGP、Diabetes Research Centre, University of Leicester
  • 主任研究者:Prof Sabyasachi Bhaumik, FRCPsych、Learning Disability Service, Leicester Partnership NHS Trust

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始

2013年2月1日

一次修了 (実際)

2015年9月1日

研究の完了 (実際)

2015年9月1日

試験登録日

最初に提出

2015年7月29日

QC基準を満たした最初の提出物

2015年7月30日

最初の投稿 (見積もり)

2015年7月31日

学習記録の更新

投稿された最後の更新 (見積もり)

2016年1月21日

QC基準を満たした最後の更新が送信されました

2016年1月20日

最終確認日

2015年7月1日

詳しくは

本研究に関する用語

この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。

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