Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
UNKNOWN
NA
120 participants
INTERVENTIONAL
2018-10-29
2020-05-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
IMPACT OF DIABETES HEALTHCARE PROGRAM ON GLYCEMIC CONTROL AND SELF-EFFICACY AMONG TYPE-II DIABETICS IN ISLAMABAD PAKISTAN
NCT06719076
Promoting Self-management Behaviors in Adolescents With Type 1 Diabetes, Using Digital Storytelling
NCT04608058
Study on the Improvement of Metabolic Indicators in Type 1 Diabetes Patients
NCT07144696
HIT on Hypoglycemic Risk in Type 1 Diabetes (T1D)
NCT03598400
Type 1 Diabetes Virtual Self-management Education and Support
NCT05756829
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
FACTORIAL
OTHER
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Routine Care
This group will be followed up for routine care, maintaining a standard log book for documenting blood sugar and insulin dosages per advice and explanation by doctors, nurses and nutritionists.
No interventions assigned to this group
e-device for step count (fit-bit)
This group will receive e-device for step count (fit-bit) in addition to routine care.
e-device for step count (fit-bit)
Patients in this group will receive fitbit device to count their daily steps and record it into their log books.
e-messages for log book
This group will receive daily e-messages for maintaining log book in addition to routine care.
e-messages for log book
Patients in this group will receive e-messages to maintain their log books as per instruction for blood sugar levels and send back weekly through snap shot.
e-messages for log book & fit-bit
This group will receive e-device for step count (fit-bit), daily e-messages for maintaining log book for blood sugar, insulin dosages and step count in addition to routine care.
e-device for step count (fit-bit)
Patients in this group will receive fitbit device to count their daily steps and record it into their log books.
e-messages for log book & fit-bit
Patient in this group will receive e-messages to maintain their log books for blood sugar levels as well as use fitbit device and maintain their log book for daily step count and send back weekly through snap shot.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
e-device for step count (fit-bit)
Patients in this group will receive fitbit device to count their daily steps and record it into their log books.
e-messages for log book
Patients in this group will receive e-messages to maintain their log books as per instruction for blood sugar levels and send back weekly through snap shot.
e-messages for log book & fit-bit
Patient in this group will receive e-messages to maintain their log books for blood sugar levels as well as use fitbit device and maintain their log book for daily step count and send back weekly through snap shot.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Patient's age ≥ 15 years
* Patient or any one of the family member like father, mother or sibling using smart phone.
* Patient or any one of the family member know how to use (receive calls or read text message) a smart phone.
Exclusion Criteria
* Pregnant females,
* Patient with neurodevelopmental delay or thalassemia
* Patient currently using any kind of authentic e-device for step count or physical activity.
15 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Aga Khan University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Syed Iqbal Azam
Assistant Professor
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Iqbal Azam, MSc
Role: PRINCIPAL_INVESTIGATOR
Aga Khan University
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Aga Khan University Hospital
Karachi, Sindh, Pakistan
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
References
Explore related publications, articles, or registry entries linked to this study.
Sawani S, Siddiqui AR, Azam SI, Humayun K, Ahmed A, Habib A, Naz S, Tufail M, Iqbal R. Lifestyle changes and glycemic control in type 1 diabetes mellitus: a trial protocol with factorial design approach. Trials. 2020 Apr 20;21(1):346. doi: 10.1186/s13063-020-4205-7.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
5363-CHS-ERC-18
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.