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Prohealth@Home: A Feasibility Study Investigating the Use of a Lifestyle App in People at Risk of Type 2 Diabetes

Primary Purpose

Pre-diabetes

Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Lifestyle counselling
Sponsored by
University of Plymouth
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Pre-diabetes

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Diagnosed with prediabetes
  • 18 years or over
  • Access to the internet and a computer/ipad or smart phone

Exclusion Criteria:

  • Diabetes (Type 1 or Type 2)
  • Less than 18 years of age
  • Treated with metformin
  • Mental health problems
  • Pregnant
  • Following a special diet
  • Already participating in another study
  • No internet access, computer/ipad or smart phone

Sites / Locations

  • University of Plymouth

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Lifestyle counselling

Arm Description

This will consist of a web-based lifestyle app and personalised behaviour modification advice by a registered dietitian delivered via messaging.

Outcomes

Primary Outcome Measures

Participants acceptability of intervention by focus group
Participants will be invited to attend a focus group at the end of the 6 month intervention period

Secondary Outcome Measures

Blood biochemistry (HbA1c, FBG, Lipids, LFT) by blood test
The blood test will be taken by a practice nurse at the GP practices and sent off for analysis as per normal protocol
Body weight and height to BMI and waist circumference by anthropometric measures
Anthropometric measures will be taken by the research assistant
Blood pressure by sphygmomanometer
A practice nurse will take the blood pressure measurements
Health status, well being, food intake and exercise levels by questionnaires
A number of questionnaires will be used to assess these parameters

Full Information

First Posted
May 13, 2015
Last Updated
April 22, 2016
Sponsor
University of Plymouth
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1. Study Identification

Unique Protocol Identification Number
NCT02450500
Brief Title
Prohealth@Home: A Feasibility Study Investigating the Use of a Lifestyle App in People at Risk of Type 2 Diabetes
Official Title
Prohealth@Home: A Feasibility Study Investigating the Application of a Web Based Lifestyle App to Improve Glycaemic Control by Changing Dietary and Activity Behaviours in Individuals at High Risk of Type 2 Diabetes
Study Type
Interventional

2. Study Status

Record Verification Date
April 2016
Overall Recruitment Status
Completed
Study Start Date
March 2015 (undefined)
Primary Completion Date
February 2016 (Actual)
Study Completion Date
February 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Plymouth

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
More than a third of the adult population in England have prediabetes, a condition that occurs when glucose levels are higher than normal but not high enough to be diagnosed as diabetes. Between 5 and 10% of people with prediabetes will go on to develop diabetes each year. Lifestyle (diet and activity) interventions have been shown to reduce the risk of prediabetes progressing to Type 2 diabetes. However, in practice high levels of professional support coupled with increasing incidence of prediabetes are not sustainable in their current format. The internet has the potential to provide an alternative means of supporting large numbers of individuals in making lifestyle changes. However, provision of information on its own is not enough to engage individuals to change - additional support via personalised feedback is required to sustain the level of motivation needed for long term behaviour change. AIM: The investigators hypothesis is that communicating with individuals at high risk of Type 2 diabetes via a web-based lifestyle app will lead to changes in lifestyle behaviours resulting in an improved glycaemic control and reduction in diabetes risk. METHOD: The study will be conducted over 6 months. Patients identified in GP practice who are at high risk of developing diabetes will be invited to take part in this feasibility study. Intervention (6 months): This will consist of a web-based lifestyle app and personalised behaviour modification advice delivered via messaging by a dietitian. Participants will also be issued with a pedometer. Data on the dietary intake and activity levels will be collected on the web-based lifestyle app. Contact between the dietitian and participants will consist of weekly messaging to facilitate changes in diet and activity behaviour through motivational and cognitive behavioural strategies. Blood biochemistry (HbA1c, FBG, LFT's and lipids), BP, weight, BMI, and waist circumference will be measured at 0, 3 and 6 months. The blood test will be taken by a practice nurse at the GP practices and sent off for analysis. A 5 day food diary, well-being and activity questionnaires will be collected at 0, 3 and 6 months by the researcher. At the end of the intervention period, participants will be invited to attend a focus group to assess participants' perceptions/ease of use and barriers to use of the technology employed to assist behaviour change
Detailed Description
Diabetes is a chronic condition. Currently there are 2.9 million people diagnosed with diabetes in the UK, with a further estimated 850,000 people who have the condition but are unaware of this (Diabetes UK, 2011). Due to the ageing population and an increase in obesity, Type 2 diabetes is increasing at an alarming rate. Diabetes UK (2011) predicts that by 2025, the number of people with diabetes will have risen to 5 million. Recent studies indicate that more than a third of the adult population in England have prediabetes (Mainous et al 2014). A condition that occurs when glucose levels are higher than normal but not high enough to be diagnosed as diabetes; between 5 and 10% of people with prediabetes will go on to develop diabetes each year (Tabak et al 2012). Lifestyle interventions aimed at making healthy dietary choices, increasing activity levels and losing excess body weight have been shown to reduce the risk of prediabetes progressing to Type 2 diabetes by 58% (Penn et al., 2013). However, in practice high levels of professional support coupled with increasing incidence of prediabetes are not sustainable in their current format. Synthesis of data from population studies, suggests a potential for less intensive interventions to be both feasible and able to reduce the risk of progressions to diabetes (Johnson et al., 2013). The internet has the potential to provide an alternative means of supporting large numbers of individuals in making diet and activity changes. However, studies highlight that information provision on its own is not enough to engage individuals to change, additional support via personalised feedback is required to sustain the level of motivation needed for long term behaviour change (Estabrook et al., 2005; Nes et al., 2013). The investigators hypothesis is that communicating with individuals at high risk of Type 2 diabetes via a web-based lifestyle app will lead to changes in lifestyle behaviours (diet and activity) resulting in improved glycaemic control and reduction in diabetes risk. To conduct a rigorous evaluation of this novel intervention will require a large and expensive multi-centre RCT. However, there are several areas of uncertainty which need to be removed before the investigators could conduct such a study with confidence. At the same time, the investigators wish to be reasonably certain that the intervention being tested in the larger trial has a good chance of being successful. Thus the purpose of this present study is to determine the feasibility of this web-based lifestyle app intervention in people with prediabetes hence determining the acceptability, practicability, integration and efficacy of the main study's procedures. Methods: The study will be conducted over 6 months in general practices. A convenience sample of consenting patients (n=30) registered at GP practices who are at high risk of developing diabetes will be invited to take part in this feasibility study. Intervention This will consist of a web-based lifestyle app and personalised behaviour modification advice by a registered dietitian delivered via messaging. Participants will be issued with a pedometer and instructed to wear this daily during all wakeful and non-bathing activities. Participants will access web-based material on prediabetes through the lifestyle app. Data on their dietary intake and activity levels will be collected on the web-based lifestyle app, this is password protected. Contact between the dietitian and participants will consist of weekly messaging to facilitate changes in diet and activity behaviour through motivational and cognitive behavioural strategies. Changes in diet and activity levels will be recorded as personalised goals which will be monitored and reviewed by both the participants and dietitian. In addition participants will be encouraged to complete a 5 day food diary using household measures or estimates of food portion sizes or weights (this will include weekend plus 3 week days) at 5 time points during the study (weeks 4, 8, 12, 18 and 22). The dietary data collected on an on-line food diary can be used by participants to self-monitor their progress against dietary recommendations based on guidelines from Diabetes UK and NICE (2012), which will be highlighted on the web platform. Data Collection Blood biochemistry (HbA1c, FBG, LFT's and lipids), BP, weight, height, BMI and waist circumference will be measured at baseline, 3 and 6 months. The blood test will be taken by a practice nurse at the GP practices and sent off for analysis. Five day food diary (5 consecutive day period including weekend plus 3 week days using a 24hr food diary) and activity questionnaire (plus data for 7 days via the activity tracker) will be collected at baseline, 3 and 6 months. To minimise contamination the first 2 days of activity data will be discarded. A follow up telephone interview will be conducted to enhance accuracy of the food diaries. This method is more responsive to dietary changes than food frequency questionnaires and is recommended for assessing intervention-related dietary change (Harris et al., 2011). The following questionnaire data will be collected at baseline, 3 and 6 months: Functional Health Status will be measured using the validated Medical Outcomes Study 36-item Short-Form Survey (SF-36) (Ware and Sherbourne, 1992). WHO wellbeing index a 5 item questionnaire will monitor changes in psychological well-being in relation to a change in treatment regimen and screen for depression (Hajos et al., 2013). ICECAP a 5 item questionnaire using a 4 item preference weighted response. It provides a broader measure of well-being for comparing the effectiveness and cost-effectiveness of the increasingly diverse array of health and social care interventions (Al-Janabi et al., 2012). Self-efficacy diet and exercise questionnaire. The perceived competence for maintaining a healthy diet and regular physical exercise are measured with four items each (Williams and Deci, 2013). International Physical Activity Questionnaire (IPAQ). Is a validated questionnaire (Craig et al., 2003) consisting of 27 questions. It measures different types of physical activity that people engage in as part of their everyday lives. Focus group: At the end of the intervention period, data will be collected via 2 focus groups, one from each recruiting GP practice, to assess patient's perceptions/ease of use and barriers to use of the technology employed to assist behaviour change and level of engagement with the technology used in this study. Data will be collected via semi-structured interviews which will be audio- recorded and then transcribed for thematic analysis.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pre-diabetes

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Lifestyle counselling
Arm Type
Experimental
Arm Description
This will consist of a web-based lifestyle app and personalised behaviour modification advice by a registered dietitian delivered via messaging.
Intervention Type
Behavioral
Intervention Name(s)
Lifestyle counselling
Intervention Description
This will consist of a web-based lifestyle app and personalised behaviour modification advice by a registered dietitian delivered via messaging. Participants will be issued with a pedometer and instructed to wear this daily. Participants will access web-based material on prediabetes through the lifestyle app. Contact between the dietitian and participants will consist of weekly messaging to facilitate changes in diet and activity behaviour through motivational and cognitive behavioural strategies. Changes in diet and activity levels will be recorded as personalised goals which will be monitored and reviewed by both the participants and dietitian. In addition participants will be encouraged to complete a food diary to self-monitor their progress against dietary recommendations.
Primary Outcome Measure Information:
Title
Participants acceptability of intervention by focus group
Description
Participants will be invited to attend a focus group at the end of the 6 month intervention period
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Blood biochemistry (HbA1c, FBG, Lipids, LFT) by blood test
Description
The blood test will be taken by a practice nurse at the GP practices and sent off for analysis as per normal protocol
Time Frame
6 months
Title
Body weight and height to BMI and waist circumference by anthropometric measures
Description
Anthropometric measures will be taken by the research assistant
Time Frame
6 months
Title
Blood pressure by sphygmomanometer
Description
A practice nurse will take the blood pressure measurements
Time Frame
6 months
Title
Health status, well being, food intake and exercise levels by questionnaires
Description
A number of questionnaires will be used to assess these parameters
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnosed with prediabetes 18 years or over Access to the internet and a computer/ipad or smart phone Exclusion Criteria: Diabetes (Type 1 or Type 2) Less than 18 years of age Treated with metformin Mental health problems Pregnant Following a special diet Already participating in another study No internet access, computer/ipad or smart phone
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Avril Collinson, PhD
Organizational Affiliation
University of Plymouth
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Plymouth
City
Plymouth
ZIP/Postal Code
PL6 8BH
Country
United Kingdom

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Participants will be provided with their biochemical results from their GPs and have access to dietary, weight and activity data through the lifestyle app.
Citations:
PubMed Identifier
23451166
Citation
Penn L, White M, Lindstrom J, den Boer AT, Blaak E, Eriksson JG, Feskens E, Ilanne-Parikka P, Keinanen-Kiukaanniemi SM, Walker M, Mathers JC, Uusitupa M, Tuomilehto J. Importance of weight loss maintenance and risk prediction in the prevention of type 2 diabetes: analysis of European Diabetes Prevention Study RCT. PLoS One. 2013;8(2):e57143. doi: 10.1371/journal.pone.0057143. Epub 2013 Feb 25.
Results Reference
background
PubMed Identifier
1593914
Citation
Ware JE Jr, Sherbourne CD. The MOS 36-item short-form health survey (SF-36). I. Conceptual framework and item selection. Med Care. 1992 Jun;30(6):473-83.
Results Reference
background
PubMed Identifier
22998334
Citation
Johnson M, Jones R, Freeman C, Woods HB, Gillett M, Goyder E, Payne N. Can diabetes prevention programmes be translated effectively into real-world settings and still deliver improved outcomes? A synthesis of evidence. Diabet Med. 2013 Jan;30(1):3-15. doi: 10.1111/dme.12018. Erratum In: Diabet Med. 2013 May;30(5):632.
Results Reference
background
PubMed Identifier
25500370
Citation
Mainous AG 3rd, Tanner RJ, Coates TD, Baker R. Prediabetes, elevated iron and all-cause mortality: a cohort study. BMJ Open. 2014 Dec 11;4(12):e006491. doi: 10.1136/bmjopen-2014-006491.
Results Reference
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PubMed Identifier
21598064
Citation
Al-Janabi H, Flynn TN, Coast J. Development of a self-report measure of capability wellbeing for adults: the ICECAP-A. Qual Life Res. 2012 Feb;21(1):167-76. doi: 10.1007/s11136-011-9927-2. Epub 2011 May 20.
Results Reference
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PubMed Identifier
12900694
Citation
Craig CL, Marshall AL, Sjostrom M, Bauman AE, Booth ML, Ainsworth BE, Pratt M, Ekelund U, Yngve A, Sallis JF, Oja P. International physical activity questionnaire: 12-country reliability and validity. Med Sci Sports Exerc. 2003 Aug;35(8):1381-95. doi: 10.1249/01.MSS.0000078924.61453.FB.
Results Reference
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PubMed Identifier
23072401
Citation
Hajos TR, Pouwer F, Skovlund SE, Den Oudsten BL, Geelhoed-Duijvestijn PH, Tack CJ, Snoek FJ. Psychometric and screening properties of the WHO-5 well-being index in adult outpatients with Type 1 or Type 2 diabetes mellitus. Diabet Med. 2013 Feb;30(2):e63-9. doi: 10.1111/dme.12040.
Results Reference
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PubMed Identifier
22683128
Citation
Tabak AG, Herder C, Rathmann W, Brunner EJ, Kivimaki M. Prediabetes: a high-risk state for diabetes development. Lancet. 2012 Jun 16;379(9833):2279-90. doi: 10.1016/S0140-6736(12)60283-9. Epub 2012 Jun 9.
Results Reference
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PubMed Identifier
23433735
Citation
Nes AA, Eide H, Kristjansdottir OB, van Dulmen S. Web-based, self-management enhancing interventions with e-diaries and personalized feedback for persons with chronic illness: a tale of three studies. Patient Educ Couns. 2013 Dec;93(3):451-8. doi: 10.1016/j.pec.2013.01.022. Epub 2013 Feb 21.
Results Reference
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Citation
Estabrooks PA, Nelson CC, Xu S, King D, Bayliss EA, Gaglio B, Nutting PA, Glasgow RE. The frequency and behavioral outcomes of goal choices in the self-management of diabetes. Diabetes Educ. 2005 May-Jun;31(3):391-400. doi: 10.1177/0145721705276578.
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Citation
Harris J, Felix L, Miners A, Murray E, Michie S, Ferguson E, Free C, Lock K, Landon J, Edwards P. Adaptive e-learning to improve dietary behaviour: a systematic review and cost-effectiveness analysis. Health Technol Assess. 2011 Oct;15(37):1-160. doi: 10.3310/hta15370.
Results Reference
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Links:
URL
http://www.nice.org.uk/guidance/ph38
Description
Preventing type 2 diabetes: risk identification and interventions for individuals at high risk [PH38]

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Prohealth@Home: A Feasibility Study Investigating the Use of a Lifestyle App in People at Risk of Type 2 Diabetes

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