Home-Based Circuit Training in Overweight/Obese Older Adult Patients With Knee Osteoarthritis and Type 2 Diabetes
NCT ID: NCT06309654
Last Updated: 2024-03-13
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
70 participants
INTERVENTIONAL
2021-09-13
2023-12-29
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 Exercise on Older Persons With Osteoarthritis
NCT00000434
Healthy Body & Mind Program for Older Adults Living With Osteoarthritis and Cognitive Decline
NCT06070818
The Effect of High Impact Exercise on Bone and Articular Cartilage in Post-menopausal Women
NCT03225703
Effects of Low-volume Aerobic Interval Training in Overweight Individuals at Increased Cardiometabolic Risk
NCT03306069
Pain & Aging: Combined Interventions for Fitness in the Community Study
NCT04099394
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Methods A total of 35 participants were required for this study after considering a dropout rate of 20%. This study involved 69 patients meeting the inclusion criteria as follows: i) age \>55 years, ii) diagnosed with KOA with Kellgren-Lawrence criteria grades 2 and 3, indicating moderate KOA, which was based on radiological assessments conducted by a traumatologist, iv) chronic knee pain for more than three months, v) T2DM based on fasting plasma glucose \>7.0 mmol·L-1 and glycated hemoglobin (HbA1c) \>6.5%, vi) overweight or obesity (BMI ≥25 kg/m2), vii) receiving the standard treatment (all patients were taking diabetes medications), and viii) providing a certificate of a negative COVID-19 diagnostic test (PCR or rapid test). Patients were excluded from the study if during the intervention they demonstrated i) secondary KOA, ii) acute knee pain, iii) changes in medication, supplementation, and/or diet, iv) changes in habitual physical activity, v) intraarticular hyaluronic acid injection treatment within one year, vi) smoking, vii) dementia or any psychiatric diseases, viii) adherence to less than 90% of total prescribed exercise sessions, or ix) they tested positive for COVID-19. After informed written consent, patients were asked not to engage in any other forms of exercise and to maintain their current habitual physical activity levels and eating patterns throughout a 3-month intervention period. Thus, the participants' logbook was reviewed at each visit, aiming to ensure that no changes in nutritional behavior and physical activity patterns occurred. CON followed standard treatment (diabetes medications) without engaging in any structured exercise throughout the intervention.
Study design This is a pragmatic randomized controlled trial study registered at the National Medical Research Register (ID: RSCH ID-21-01180-KGTNMRR ID-21-02367-FUM). The patients were recruited via a poster distributed in the Orthopedics Clinic at USM Hospital. Written informed consent was obtained from all participants before the study. Those willing to participate were then selected and randomly assigned to CON or HBCT. More specifically, patients were divided into two groups performed by an independent statistician using computer-generated random allocation sequences
Assessment procedures All patients were instructed to avoid consuming caffeinated beverages and strenuous exercise 24 hours before the first visit. A total of three visits were performed and all outcomes were assessed through the three visits (baseline, weeks 6 and 12). All measurements were performed at USM Hospital. During the first visit (baseline), assessments were carried out for cardiovascular parameters \[e.g., resting heart rate (RHR), systolic (SBP) and diastolic (DBP) blood pressure\], BMI, biomarkers \[e.g., HbA1c, interleukin 6 (IL-6), and superoxide dismutases (SOD)\], rate of perceived exertion (RPE), blood oxygen levels (SpO2), and a 6-minute walk test (6MWT) to assess cardiorespiratory fitness (CRF). KOA symptoms and comorbidity score were also assessed. During the second visit at week 6 (mid-testing), an assessment of cardiovascular parameters and KOA symptoms, RPE, SpO2, and 6MWT took place. During the third visit at week 12 (post-testing), similar assessments to those conducted at baseline were carried out.
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
PARALLEL
TREATMENT
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
home-based circuit training (HBCT) protocol
Participants in the exercise group performed HBCT three times per week on non-consecutive days for 12 weeks.
12-week home-based circuit training (HBCT)
Participants in the exercise group performed HBCT three times per week on non-consecutive days for 12 weeks. The first session was conducted at USM Hospital and participants were instructed how to perform the prescribed exercises in a correct form. In each session, participants performed seven exercises (two aerobic- and five resistance-based) in a circuit fashion, using bodyweight movements and adjustable dumbbells for varied weights, activating all the major muscle groups. In weeks 1-6, participants executed 15 repetitions for 2 rounds with 1 min passive rest between exercises and rounds. In weeks 7-12, participants executed 30 repetitions for 4 rounds with the same rest as prescribed in weeks 1-6. Each round lasted 10-15 min and the total session duration was 20-60 min, aiming to help participants adapt gradually to increasing training volume.
Standard of care (CONT)
Providing education about the nature of OA, its progression, and strategies for symptom management.
Empowering individuals with self-management techniques, such as joint protection strategies, activity modification, and lifestyle changes (e.g., weight management, exercise).
Standard of care (CONT)
Providing education about the nature of OA, its progression, and strategies for symptom management.
Empowering individuals with self-management techniques, such as joint protection strategies, activity modification, and lifestyle changes (e.g., weight management, exercise).
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
12-week home-based circuit training (HBCT)
Participants in the exercise group performed HBCT three times per week on non-consecutive days for 12 weeks. The first session was conducted at USM Hospital and participants were instructed how to perform the prescribed exercises in a correct form. In each session, participants performed seven exercises (two aerobic- and five resistance-based) in a circuit fashion, using bodyweight movements and adjustable dumbbells for varied weights, activating all the major muscle groups. In weeks 1-6, participants executed 15 repetitions for 2 rounds with 1 min passive rest between exercises and rounds. In weeks 7-12, participants executed 30 repetitions for 4 rounds with the same rest as prescribed in weeks 1-6. Each round lasted 10-15 min and the total session duration was 20-60 min, aiming to help participants adapt gradually to increasing training volume.
Standard of care (CONT)
Providing education about the nature of OA, its progression, and strategies for symptom management.
Empowering individuals with self-management techniques, such as joint protection strategies, activity modification, and lifestyle changes (e.g., weight management, exercise).
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* diagnosed with KOA with Kellgren-Lawrence criteria grades 2 and 3, indicating moderate KOA, which was based on radiological assessments conducted by a traumatologist
* chronic knee pain for more than three months
* T2DM based on fasting plasma glucose \>7.0 mmol·L-1 and glycated hemoglobin (HbA1c) \>6.5%,
* overweight or obesity (BMI ≥25 kg/m2)
* providing a certificate of a negative COVID-19 diagnostic test (PCR or rapid test).
Exclusion Criteria
* acute knee pain,
* changes in medication, supplementation, and/or diet
* changes in habitual physical activity
* smoking
* dementia or any psychiatric diseases
* adherence to less than 90% of total prescribed exercise sessions
* tested positive for COVID-19
55 Years
75 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Princess Nourah Bint Abdulrahman University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Monira Aldhahi
Associate professor
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Sameer Al-Mhanna, Phd
Role: STUDY_DIRECTOR
Department of physiology, School of Medical Sciences, Universiti Sains Malaysia, Kubang Kerian 16150, Kelantan, Malaysia
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Princess Nourah bint Abdulrahman University
Riyadh, , 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.
PNU
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.