Differential Air Pressure Technology for Treatment of Diabetic Elderly Patients
NCT ID: NCT04620265
Last Updated: 2020-11-06
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.
COMPLETED
NA
110 participants
INTERVENTIONAL
2020-03-01
2020-10-01
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
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
TREATMENT
DOUBLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Treadmill training 100%
This group received antigravity treadmill training 100% weight bearing and conventional exercise program.
Antigravity treadmill training 100% weight bearing
This group received antigravity treadmill training 100% weight bearing and conventional exercise program.
The conventional exercise program
This group received the conventional exercise program only.
Treadmill training 75%
This group received antigravity treadmill training 75% weight bearing and conventional exercise program.
Antigravity treadmill training 75% weight bearing
This group received antigravity treadmill training 75% weight bearing and conventional exercise program.
The conventional exercise program
This group received the conventional exercise program only.
Treadmill training 50%
This group received antigravity treadmill training 50% weight bearing and conventional exercise program.
Antigravity treadmill training 50% weight bearing
This group received antigravity treadmill training 50% weight bearing and conventional exercise program.
The conventional exercise program
This group received the conventional exercise program only.
Treadmill training 25%
This group received antigravity treadmill training 25% weight bearing and conventional exercise program.
Antigravity treadmill training 25% weight bearing
This group received antigravity treadmill training 25% weight bearing and conventional exercise program.
The conventional exercise program
This group received the conventional exercise program only.
Conventional program
This group received the conventional exercise program only.
The conventional exercise program
This group received the conventional exercise program only.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Antigravity treadmill training 100% weight bearing
This group received antigravity treadmill training 100% weight bearing and conventional exercise program.
Antigravity treadmill training 75% weight bearing
This group received antigravity treadmill training 75% weight bearing and conventional exercise program.
Antigravity treadmill training 50% weight bearing
This group received antigravity treadmill training 50% weight bearing and conventional exercise program.
Antigravity treadmill training 25% weight bearing
This group received antigravity treadmill training 25% weight bearing and conventional exercise program.
The conventional exercise program
This group received the conventional exercise program only.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Diagnosed as having uncontrolled Type 2 Diabetes Mellitus, with glycosylated haemoglobin (HbA1c) level between 7 and 11 and fasting glucose level ranged from 7.0 -11.1 mmol/L.
* Treated only with oral anti-diabetic agents (not taking insulin),
* Pharmacological treatment had to be stable for at least 3 months before the study.
* They will be selected among old subjects that were able to walk independently with or without assistive device but with poor balance
Exclusion Criteria
* Patients who had got a score over 19 according to Tinetti scale of balance assessment,
* Patient with malnutrition (BMI \< 21 kg/m2 or with recent weight loss \> 5% body weight in the last month or \> 10% in six months),
* Patients with established hypertension (resting systolic blood pressure \> 140 mmHg and diastolic blood pressure \> 90 mmHg,
* With any severe chronic or uncontrolled comorbid condition as recent myocardial infarction, unstable angina, acute congestive heart failure, third degree heart block and uncontrolled arrhythmia.
* Patients will be excluded also if they have abnormal skin integrity e.g. wound or scare tissues or are on other complementary treatment,
* History of serious cerebrovascular or cardiovascular diseases, and severe debilitating musculoskeletal problems).
60 Years
80 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Umm Al-Qura University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Shamekh Mohamed El-Shamy
Professor
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Shamekh M El-Shamy, Ph.D.
Role: PRINCIPAL_INVESTIGATOR
Professor
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Al Noor Specialized Hospital
Mecca, , Saudi Arabia
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
Umm AlQura Univ
Identifier Type: -
Identifier Source: org_study_id