A Nurse-led Smartphone-based Self-management Programme for Type 2 Diabetes Patients With Poor Blood Glucose Control
Primary Purpose
Type2 Diabetes Mellitus
Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
nurse-led smartphone-based self-management programme
exiting nurse-led diabetes service
Sponsored by
About this trial
This is an interventional other trial for Type2 Diabetes Mellitus
Eligibility Criteria
Inclusion Criteria:
- have confirmed medical diagnosis of type 2 DM;
- are 21 years old and above;
- have blood test result of HbA1c > 8% in the most recent test indicating poor glycemic control;
- possess and able to use smart mobile phone (e.g. Samsung Galaxy, iPhone) in their daily lives; and
- are able to speak and read English or Chinese.
Exclusion Criteria:
- have suffered severe complications such as severe stroke, visual impairment, renal failure that interfere with self-care activities;
- have known history of major psychiatric illness;
- have reading and hearing difficulties.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Experimental Group
Control Group
Arm Description
A six-month nurse-led smartphone-based self-management programme (i.e. NSSMP) will be provided to the participants in the experimental group.
the patients in the control group will receive the exiting nurse-led diabetes service (i.e. NDS) provided by the hospital
Outcomes
Primary Outcome Measures
Self-efficacy: change is being assessed
Self-efficacy will be assessed using the General Self-efficacy Scale (GSS), a 10-item questionnaire of the unidimensional measure of one's competence to deal with the challenging events encountered in various life situations
Secondary Outcome Measures
Diabetes self-care activities: change is being assessed
Diabetes self-care activities will be measured using the 11-item Revised Summary of Diabetes Self-care Activities (RSDSCA)
Health-related Quality of Life: change is being assessed
Health-related Quality of Life will be measured using the 19-item Diabetes-Dependent Quality of Life (DDQoL)
Acute Diabetes Complications: change is being assessed
the number of frequency of acute diabetes complications including hypoglycaemia, DKA and HHS will be collected
HbA1c: change is being assessed
HbA1c will be obtained from patient's medical record
Smoking status: change is being assessed
Smoking status will reported by the participant.
Alcohol consumption: change is being assessed
Alcohol consumption will be reported by the participant
Diabetes-related hospital admission
number of diabetes-related hospital admission will be recorded
Visits to the emergency
number of diabetes-related emergency department visit will be recorded
Unplanned medical consultation
number of unplanned medical consultation due to diabetes problems will be recorded
Full Information
NCT ID
NCT03088475
First Posted
March 13, 2017
Last Updated
March 16, 2017
Sponsor
National University of Singapore
Collaborators
National University Hospital, Singapore
1. Study Identification
Unique Protocol Identification Number
NCT03088475
Brief Title
A Nurse-led Smartphone-based Self-management Programme for Type 2 Diabetes Patients With Poor Blood Glucose Control
Official Title
A Randomised Controlled Trial on a Nurse-led Smartphone-based Self-management Programme for Type 2 Diabetes Patients With Poor Glycaemic Control
Study Type
Interventional
2. Study Status
Record Verification Date
March 2017
Overall Recruitment Status
Unknown status
Study Start Date
January 1, 2018 (Anticipated)
Primary Completion Date
June 30, 2019 (Anticipated)
Study Completion Date
December 30, 2019 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
National University of Singapore
Collaborators
National University Hospital, Singapore
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Aim. To develop and compare a nurse-led smartphone-based self-management programme with an existing nurse-led diabetes service on health-related outcomes of type 2 diabetes patients with poor glycaemic control in Singapore.
Background. Over the past decades, Asia has emerged as the 'diabetes epicentre' in the world due to rapid economic development, urbanisation, and nutrition transition. There is an urgent need to develop more effective care management strategies in response to this rising diabetes epidemic.
Design. A randomised controlled trial with pre- and repeated post-tests control group design.
Methodology. A total of 128 type 2 diabetes patients with poor glycaemic control will be recruited from the diabetes clinic of a public acute hospital in Singapore through convenience sampling. Study participants will be randomly allocated either to the experimental group or the control group. Outcome measures will include the 10-item General Self-Efficacy Scale, 11-item Revised Summary of Diabetes Self-care Activities, and 19-item Diabetes-Dependent Quality of Life. Data will be collected at three time points: baseline, 3 months, and 6 months from the baseline.
Discussion. It is expected that this programme will be an alternative offered to diabetes patients to master their self-care management skills, in addition to the existing diabetes service provided in diabetes clinics in Singapore hospitals. Furthermore, the self-supporting and less resource-intensive nature of this programme, through the use of a smartphone application as the mode of intervention delivery, will greatly reduce nurses' direct contact time with patients and allow more time to be allocated to those who require more attention.
Detailed Description
Specific Aims
The aims of this study are:
to develop a nurse-led smartphone-based self-management programme (NSSMP) for patients with type 2 diabetes;
to compare the NSSMP with an existing nurse-led diabetes service (NDS) on self-efficacy, diabetes self-care activities, health-related quality of life (HRQoL), glycaemic control, acute diabetes complications (e.g. hypoglycaemia, Diabetic Ketoacidosis [DKA] and Hyperosmolar Hyperglycemic Syndrome [HHS]), and health-service use among type 2 diabetes patients with poor glycemic control in Singapore.
Study Hypotheses
Study participants will be randomized into an existing NDS group (i.e. control group) and a newly developed NSSMP group (i.e. experimental group). It is hypothesized that participants in the NSSMP group as compared with participants in the NDS group will have significantly:
Higher level of self-efficacy;
Increased level of diabetes self-care activities;
More positive perceived health-related quality of life;
Reduced glycosylated haemoglobin (HbA1c) and acute diabetes complications (e.g. hypoglycaemia, Diabetic Ketoacidosis [DKA] and Hyperosmolar Hyperglycemic Syndrome [HHS] ); and
Reduced usage of health services (e.g. diabetes-related hospital readmission, emergency room attendance, and unplanned medical consultation).
Approach Adopted in This Study Development of NSSMP: A nurse-led smartphone-based self-management programme, or NSSMP for short, will be developed by the study team. The model of self-efficacy will be used to guide the development of the NSSMP to ensure it would be theoretically sound and empirically tested. The NSSMP is a 6-month programme comprising an individual education session, and a newly developed smartphone App as a self-help education resource. The NSSMP involves the use of a smartphone, internet, and communication technologies to assist patients to manage their disease at homes or wherever they are. Patient's health data will be monitored by their smartphones. All the data will be synchronized to a web-connected portal on a remote server. The nurse would be able to access the participant's data (e.g. blood glucose, exercise, blood pressure, body weight, diet) through the web-connected portal so that the individualized care and consultation could be rendered through the tele or video conference.
Study design, setting and participants: A randomized controlled trial with a pre- and repeated post-test control group design is adopted. A convenience sample of 128 type 2 DM patients with poor glycemic control will be recruited from the Diabetes Clinic of National University Hospital (NUH). Study participants will be randomly assigned either to a 6-month NSSMP group (i.e experimental group) or the NDS group (i.e. control group). The existing NDS for DM patients in the NUH consists of face-to-face patient education sessions plus telephone follow-ups. The patients are required to return back to the Diabetes Clinic to attend the educations sessions based on the scheduled appointment. They are instructed to measure blood glucose at home and modes of contact (voicemail, fax and email address) are given for reporting the glucose readings weekly. If the patient does not report, the nurse will have to make calls or send SMS message to the patient to follow up their blood glucose results. The nurses would then provide telephone counselling services to the patients where needed based on the blood glucose results, and sometime would request patients coming back to the Diabetes Clinic to see the doctors and the diabetes advanced practice nurses.
Outcome measures: Study outcome measures include the 10-item General Self-Efficacy Scale, 11-item Revised Summary of Diabetes Self-care Activities, and 19-item Diabetes-Dependent Quality of Life which will be used to measure self-efficacy, level of diabetes self-care activities, and health-related quality of life of the participants respectively. The participant's socio-demographic and clinical data (e.g. HbA1c, acute diabetes complications, and lipid level) will be also collected. Data will be collected at 3 time points: baseline (i.e. pre-test), 3 months from baseline (post-test 1), and 6 months from the baseline (post-test 2). The health service use (e.g. diabetes-related hospital readmission, emergency room attendance, and unplanned medical consultation) will be also assessed at the 6th month of the end of the programme.
Data analysis: The IBM SPSS 23.0 will be used for data entry and analysis. Intention-to-treat will be adopted in data analysis. Repeated measures analysis of covariance will be used to examine the differences between, within, and the interaction (group x time) effects on each continuous outcome. Confounding variables (e.g. age), will be controlled as covariate in the analysis. The Chi-squared test or Fisher's exact test will be used to test the difference of the incidence of acute diabetes complications and the numbers of health service use between the two groups. All statistical tests will be two-tailed, and a p < 0.05 is used to indicate statistical significance.
Study Significance If the NSSMP is demonstrated to be effective in this study, a smartphone App developed in this project can be provided to all DM patients and their family members/caregivers as a self-help education resource at home. It will provide and equip knowledge to the patient and their family members/caregivers to enhance their knowledge and skills in management of diabetes so as to achieve the expected patient outcomes in improving self-efficacy, diabetes self-care activities, HRQoL, and clinical outcomes. It is expected that this programme will be an option that can be offered to diabetes patients to master their self-care management skills in addition to the existing diabetes service provided in diabetes clinics in Singapore hospitals where patients with poorly controlled condition are being monitored. In addition, the independent nature of this programme with application of technology will greatly reduce nurses' contact time with patients which accord them more time for those who require more time, for example, those afflicted with diabetes-related complications. This will result in a more efficient use of healthcare resources in the long run. Eventually, this programme will be available for all diabetes patients living in the community.
Feasibility of the Study The research team comprises experienced researchers from different disciplines. The PI has extensive research experience in the area of chronic diseases management and mHealth intervention. Two Co-Is are practised clinicians in diabetes care, they will facilitate the access to potential study participants and oversee the implementation of the project. One Co-I has the expertise in biomedical engineering, mobile App development, and information management. He and his team will be in charge of developing the system. In addition, the preliminary integrative literature review and qualitative patient interviews were performed to inform the development of the content for the mobile app. Through harnessing the technology, the smartphone App based platform can be established to reduce the contact time with patients for the healthcare providers.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Type2 Diabetes Mellitus
7. Study Design
Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
128 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Experimental Group
Arm Type
Experimental
Arm Description
A six-month nurse-led smartphone-based self-management programme (i.e. NSSMP) will be provided to the participants in the experimental group.
Arm Title
Control Group
Arm Type
Active Comparator
Arm Description
the patients in the control group will receive the exiting nurse-led diabetes service (i.e. NDS) provided by the hospital
Intervention Type
Behavioral
Intervention Name(s)
nurse-led smartphone-based self-management programme
Intervention Description
The participants in the experimental group will undergo nurse-led smartphone-based self-management programme (NSSMP), a 6-month programme comprising an individual education session, and a newly developed smartphone App as a self-help education resource
Intervention Type
Behavioral
Intervention Name(s)
exiting nurse-led diabetes service
Intervention Description
the patients in the control group will receive the exiting nurse-led diabetes service (i.e. NDS) provided by the hospital
Primary Outcome Measure Information:
Title
Self-efficacy: change is being assessed
Description
Self-efficacy will be assessed using the General Self-efficacy Scale (GSS), a 10-item questionnaire of the unidimensional measure of one's competence to deal with the challenging events encountered in various life situations
Time Frame
Change from baseline self-efficacy at 6 months
Secondary Outcome Measure Information:
Title
Diabetes self-care activities: change is being assessed
Description
Diabetes self-care activities will be measured using the 11-item Revised Summary of Diabetes Self-care Activities (RSDSCA)
Time Frame
Change from baseline diabetes self-care acitivities at 6 months
Title
Health-related Quality of Life: change is being assessed
Description
Health-related Quality of Life will be measured using the 19-item Diabetes-Dependent Quality of Life (DDQoL)
Time Frame
Change from baseline health-related quality of life at 6 months
Title
Acute Diabetes Complications: change is being assessed
Description
the number of frequency of acute diabetes complications including hypoglycaemia, DKA and HHS will be collected
Time Frame
Change from baseline acute diabetes complications at 6 months
Title
HbA1c: change is being assessed
Description
HbA1c will be obtained from patient's medical record
Time Frame
Change from baseline HbA1c at 6 months
Title
Smoking status: change is being assessed
Description
Smoking status will reported by the participant.
Time Frame
Change from baseline smoking status at 6 months
Title
Alcohol consumption: change is being assessed
Description
Alcohol consumption will be reported by the participant
Time Frame
Change from baseline alcohol consumption at 6 months
Title
Diabetes-related hospital admission
Description
number of diabetes-related hospital admission will be recorded
Time Frame
at the 6-month of the study period
Title
Visits to the emergency
Description
number of diabetes-related emergency department visit will be recorded
Time Frame
at the 6-month of the study period
Title
Unplanned medical consultation
Description
number of unplanned medical consultation due to diabetes problems will be recorded
Time Frame
at the 6-month of the study period
10. Eligibility
Sex
All
Minimum Age & Unit of Time
21 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
have confirmed medical diagnosis of type 2 DM;
are 21 years old and above;
have blood test result of HbA1c > 8% in the most recent test indicating poor glycemic control;
possess and able to use smart mobile phone (e.g. Samsung Galaxy, iPhone) in their daily lives; and
are able to speak and read English or Chinese.
Exclusion Criteria:
have suffered severe complications such as severe stroke, visual impairment, renal failure that interfere with self-care activities;
have known history of major psychiatric illness;
have reading and hearing difficulties.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Wenru P Wang, PhD
Phone
65 66011761
Email
nurww@nus.edu.sg
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Wenru P Wang, PhD
Organizational Affiliation
National University of Singapore
Official's Role
Principal Investigator
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
35170786
Citation
Jiang Y, Ramachandran HJ, Teo JYC, Leong FL, Lim ST, Nguyen HD, Wang W. Effectiveness of a nurse-led smartphone-based self-management programme for people with poorly controlled type 2 diabetes: A randomized controlled trial. J Adv Nurs. 2022 Apr;78(4):1154-1165. doi: 10.1111/jan.15178. Epub 2022 Feb 15.
Results Reference
derived
PubMed Identifier
28727183
Citation
Wang W, Seah B, Jiang Y, Lopez V, Tan C, Lim ST, Ren H, Khoo YH. A randomized controlled trial on a nurse-led smartphone-based self-management programme for people with poorly controlled type 2 diabetes: A study protocol. J Adv Nurs. 2018 Jan;74(1):190-200. doi: 10.1111/jan.13394. Epub 2017 Aug 17.
Results Reference
derived
Learn more about this trial
A Nurse-led Smartphone-based Self-management Programme for Type 2 Diabetes Patients With Poor Blood Glucose Control
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