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Pre-diabetesNCT02450500

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

A study testing Lifestyle counselling in people with Pre-diabetes, run by University of Plymouth at 1 site in United Kingdom.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial 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. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Pre-diabetes
What is being tested?
Lifestyle counselling
Could I receive a placebo?
No, everyone receives an active treatment
How many people
10 participants
Where
1 siteUnited Kingdom
Study dates
Mar 2015to Feb 2016
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

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

Who cannot join

  • 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

Trial locations and contacts

1 site in 1 country.

United Kingdom1 site
  • University of Plymouth

    Plymouth, PL6 8BH

Other trials in United Kingdom

About this study

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

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.

Read more

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

Read the 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.

Conditions
Pre-diabetes
Being tested
Lifestyle counselling
Medical subject headings
Glucose Intolerance

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Lifestyle counsellingBehavioural

    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.

Study groups in NCT02450500
Study groupRoleWhat they receive
Lifestyle counsellingExperimentalThis will consist of a web-based lifestyle app and personalised behaviour modification advice by a registered dietitian delivered via messaging.
Receives: Behavioral: Lifestyle counselling

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. 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

    Measured: 6 months

Secondary outcomes (4)
  1. 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

    Measured: 6 months

  2. Body weight and height to BMI and waist circumference by anthropometric measures

    Anthropometric measures will be taken by the research assistant

    Measured: 6 months

  3. Blood pressure by sphygmomanometer

    A practice nurse will take the blood pressure measurements

    Measured: 6 months

  4. Health status, well being, food intake and exercise levels by questionnaires

    A number of questionnaires will be used to assess these parameters

    Measured: 6 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted21 May 2015 (estimated)
  2. Study startMar 2015
  3. Primary completionFeb 2016
  4. Study completionFeb 2016

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Prevention
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
10 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02450500
Sponsor's protocol ID
14/SW/1047
Status last verified
Apr 2016
First submitted
13 May 2015
Last updated
25 Apr 2016
Results posted
No
Data monitoring committee
No
Individual data sharing
Yes: Participants will be provided with their biochemical results from their GPs and have access to dietary, weight and activity data through the lifestyle app.

Publications

  • 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.

    PubMed 23451166
  • 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.

    PubMed 1593914
  • 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.

    PubMed 22998334
  • 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.

    PubMed 25500370
  • 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.

    PubMed 21598064
  • 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.

    PubMed 12900694
  • 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.

    PubMed 23072401
  • 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.

    PubMed 22683128
  • 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.

    PubMed 23433735
  • 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.

    PubMed 15919639
  • 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.

    PubMed 22030014

Questions about this trial

What is this clinical trial studying?

A study testing Lifestyle counselling in people with Pre-diabetes, run by University of Plymouth at 1 site in United Kingdom.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 8 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 25 Apr 2016. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United Kingdom. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Participants acceptability of intervention by focus group (time frame: 6 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT02450500, which also lists 11 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 25 Apr 2016.

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