Obesity Clinical Trial
— I-careOfficial title:
I-care: Stimulating Self-management in Patients With Type 2-diabetes Through Web-based Situational Feedback. A Pilot Study.
NCT number | NCT01297049 |
Other study ID # | 2010/427b |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | April 2010 |
Est. completion date | December 2015 |
Verified date | September 2018 |
Source | Oslo and Akershus University College of Applied Sciences |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The overall objective of this pilot study is to develop a cost-effective treatment methodology delivered outside of traditional clinical setting, and based on modern technology for patients with diabetes type 2 also suffering from obesity. This study will investigate the feasibility of web based counselling and situational feedback through mobile supervising. The intention is to treat 10-15 patients. All participants will receive standard treatment delivered by their general practitioners. In addition the participants will fill in and send diaries to the supervisors each evening for 4 weeks reduced to a weekly frequency for the next two months period. The diary's schedule will be an evaluation of the day activities related to meals and food, medication management as well as the performed physical activities. The diary's schedule will also include blood glucose sample, and plans for the next day especially regarding physical activity. The participants will be able to view their own registrations on a web page. Daily/weekly situational feedback will be given to the participants within a cognitive behavioural framework to stimulate self-management. The primary outcome will be the HbA1c levels. Secondary outcomes will include evaluation of lifestyle outcomes such as physical activity levels and eating behaviour, and skills such as self-management of medication. In addition, the interventions effectiveness will examine mental health outcomes such as emotional distress and health-related quality of life.
Status | Completed |
Enrollment | 15 |
Est. completion date | December 2015 |
Est. primary completion date | July 2015 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 70 Years |
Eligibility |
Inclusion Criteria: - age 18-70 years old - T2DM diagnosed > 3 months prior to study - HbA1c 7,5-10% - capability of filling in Norwegian questionnaires - BMI = 25 - able and willing to give signed informed consent - willing to attend the full treatment schedule including ability to use mobile phones, computers and pocket computers Exclusion Criteria: - change in weight > 5kg during the last 3 months - any mental or physical condition interfering with the protocol - not having easy access to computers - having reading problems |
Country | Name | City | State |
---|---|---|---|
Norway | Oslo College University | Oslo | Arkeshus |
Lead Sponsor | Collaborator |
---|---|
Oslo and Akershus University College of Applied Sciences | University of Oslo |
Norway,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Blood glucose control with changes in Glycated hemoglobin (HbA1c) values | HBA1c is a form of hemoglobin used primarily to identify the average plasma glucose concentration over prolonged periods of time. It is formed in a non-enzymatic glycation pathway by hemoglobin's exposure to plasma glucose. Normal levels of glucose produce a normal amount of glycated hemoglobin. As the average amount of plasma glucose increases, the fraction of glycated hemoglobin increases in a predictable way. This serves as a marker for average blood glucose levels over the previous months prior to the measurement | At the baseline and at the end of the intervention (3 months) | |
Secondary | Health Education Impact Questionnaire (heiQ); | heiQ is a user-friendly instrument for the comprehensive evaluation of patient education programs with the following dimensions: positive and active engagement in life, health directed behavior, skill and technique acquisition, constructive attitudes and approaches, self-monitoring and insight, health service navigation, social integration and support, and emotional well-being. | At the baseline and after the end of the intervention (3 months) | |
Secondary | Problem Areas in Diabetes (PAID) | PAID is a brief self-report measure of diabetes-related distress that has been found to be useful in patients with diabetes (both type1 and 2). PAID scores have been found to show positive associations with HbA1c, and are a major predictor of poor adherence to treatment not involving general emotional distress | At the baseline and after the end of the intervention (3 months) | |
Secondary | Food frequency questionnaire FFQ | FFQ is a measure designed to measure average long-term diet or usual consumption with specified food items. | At the baseline and after the end of the intervention (3 months) | |
Secondary | Audit of Diabetes Dependence Quality of Life (ADDQoL-19) | ADDQoL19 is a health-related quality of life questionnaire well designed to assess to what extent diabetes may affect different aspects of health related quality of life. The ADDQoL includes 2 introductory questions and 18 specific items, with the purpose of assessing, according to the patient's perspective, how much better his or her life would be if he/she did not have diabetes and how important each of these 19 aspects of life are for the individual. | At the baseline and after the end of the intervention (3months) |
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