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Assessing the Effectiveness of Diabetes Interactive Diary (DID) in Diabetes Management (DID)

Primary Purpose

Type 1 Diabetes Mellitus

Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
A software programme in mobile telephone
Standard Education Programme.
Sponsored by
The Royal Bournemouth Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Type 1 Diabetes Mellitus

Eligibility Criteria

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

Inclusion Criteria:

  • Aged 18 or over
  • Not habitually using carbohydrate counting and insulin dose adjustment
  • Testing their blood sugar levels at least 3 times a day
  • Using multiple daily injections of short-acting and long-acting insulin analogues
  • With HbA1c between 7.5% and 10%
  • Familiar with the use of mobile phones and possess a personal SIM card.

Exclusion Criteria:

  • Mental conditions, depression or high anxiety rendering the subject unable to understand the nature, scope, and possible consequences of the study
  • Eating disorders
  • Pregnancy
  • Any clinically significant major organ system disease or infective diseases
  • Any disease or condition or abuse of illicit drugs, prescription medicines or alcohol that in the opinion of the investigator may interfere with the completion of the study
  • Subject unlikely to comply with protocol, e.g., uncooperative attitude, inability to return for follow-up visits and unlikely to complete the study procedures

Sites / Locations

  • Royal Bournemouth Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

1

2

Arm Description

To assess the efficacy of a Diabetes Interactive Diary in Diabetes Management.

Control Arm. Patients will receive standard education programme.

Outcomes

Primary Outcome Measures

The difference in HbA1c between the patient in the DID group and in the standard education group.

Secondary Outcome Measures

The differences between the two groups in terms of, lipid profile, blood pressure, the number of hypoglycaemic episodes, daily blood sugar fluctuation, total insulin dose, weight changes and patients' satisfaction with the treatment.

Full Information

First Posted
June 4, 2007
Last Updated
July 8, 2008
Sponsor
The Royal Bournemouth Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT00482443
Brief Title
Assessing the Effectiveness of Diabetes Interactive Diary (DID) in Diabetes Management
Acronym
DID
Official Title
A Multinational, Randomised Study of the Efficacy of the Diabetes Interactive Diary (DID), a Carbohydrates/Insulin Bolus Calculator and a Telemedicine System Based on the Communication Between Physician or Dietitian and Patient by SMS
Study Type
Interventional

2. Study Status

Record Verification Date
July 2008
Overall Recruitment Status
Completed
Study Start Date
March 2007 (undefined)
Primary Completion Date
April 2008 (Actual)
Study Completion Date
April 2008 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
The Royal Bournemouth Hospital

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
For people with Type 1 Diabetes, blood glucose control is achieved by matching insulin doses directly to the amount of carbohydrate consumed. We are looking at new ways to help our patients with type 1 diabetes manage their diabetes control more effectively. We are testing if "Diabetes Interactive Diary" (DID), a novel programme designed to be used on a mobile phone, can represent an important tool in carbohydrate counting while avoiding the use of complex calculations and in depth knowledge about the carbohydrate content of their food.
Detailed Description
This is randomized control trial aimed to evaluate the effectiveness of a DID compare to the standard education approach in order to help the patients with Type 1 diabetes to estimate the carbohydrate in their food and adjust insulin doses. It involves individuals with Type 1 diabetes who are not habitually using carbohydrate counting. They should be testing their blood sugar levels at least 3 times a day, using multiple daily injections of short-acting and long-acting insulin analogues, with HbA1c between 7.5% and 10% and are familiar with the use of mobile phones and possess a personal SIM card. Patients will be randomized to the standard education programme run for 4 full days over a 4 week period or to the DID programme run as three 2-hour sessions over a two-week period. The DID is a novel software programme installed on the patient's mobile telephone. It facilitates the communication between the dietitian and the patient by using SMS text messages, so that the dietitian can monitor glycaemic control and suggest adjustments if necessary. It can be described as a little computer, where the patient can record their blood glucose value, the amount of insulin injected and the amount of carbohydrate consumed.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Type 1 Diabetes Mellitus

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
20 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Description
To assess the efficacy of a Diabetes Interactive Diary in Diabetes Management.
Arm Title
2
Arm Type
Active Comparator
Arm Description
Control Arm. Patients will receive standard education programme.
Intervention Type
Other
Intervention Name(s)
A software programme in mobile telephone
Intervention Description
Use of Mobile phone technology in maintaining Diabetes Interactive Diary.
Intervention Type
Other
Intervention Name(s)
Standard Education Programme.
Intervention Description
Control Arm patients will receive a standard education programme designed to help the Type 1 Diabetic manage their condition.
Primary Outcome Measure Information:
Title
The difference in HbA1c between the patient in the DID group and in the standard education group.
Time Frame
6 month
Secondary Outcome Measure Information:
Title
The differences between the two groups in terms of, lipid profile, blood pressure, the number of hypoglycaemic episodes, daily blood sugar fluctuation, total insulin dose, weight changes and patients' satisfaction with the treatment.
Time Frame
6 month

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Aged 18 or over Not habitually using carbohydrate counting and insulin dose adjustment Testing their blood sugar levels at least 3 times a day Using multiple daily injections of short-acting and long-acting insulin analogues With HbA1c between 7.5% and 10% Familiar with the use of mobile phones and possess a personal SIM card. Exclusion Criteria: Mental conditions, depression or high anxiety rendering the subject unable to understand the nature, scope, and possible consequences of the study Eating disorders Pregnancy Any clinically significant major organ system disease or infective diseases Any disease or condition or abuse of illicit drugs, prescription medicines or alcohol that in the opinion of the investigator may interfere with the completion of the study Subject unlikely to comply with protocol, e.g., uncooperative attitude, inability to return for follow-up visits and unlikely to complete the study procedures
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
David Kerr, Doctor
Organizational Affiliation
Royal Bournemouth Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Anita Bowes, Dietitian
Organizational Affiliation
Royal Bournemouth Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Royal Bournemouth Hospital
City
Bournemouth
State/Province
Dorset
ZIP/Postal Code
BH7 7DW
Country
United Kingdom

12. IPD Sharing Statement

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Assessing the Effectiveness of Diabetes Interactive Diary (DID) in Diabetes Management

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