Clinical Trials Logo

Clinical Trial Summary

Intervention in the form of a PA (physical activity) program combining aerobic, resistance, and flexibility exercises adapted for wearing a lower limb offloading device and limiting weight-bearing on the feet, with a duration of twelve (12) weeks, consisting of two supervised sessions and one unsupervised home session per week.


Clinical Trial Description

Objectives: 1. Evaluate the acceptability of a non-weight bearing physical activity (PA) program; 2. Assess the feasibility of the PA program and the data collection procedure; 3. Evaluate the feasibility of a submaximal exercise test for cardiorespiratory capacity; and 4. Verify the sensitivity of dependent variables to respond to a physical activity program (e.g., cardiorespiratory capacity, cardiovascular and metabolic risk factors, quality of life, PA level). Type of study: Feasibility and acceptability study with a pre-post evaluative design. Intervention: Intervention in the form of a PA (physical activity) program combining aerobic, resistance, and flexibility exercises adapted for wearing a lower limb offloading device and limiting weight-bearing on the feet, with a duration of twelve (12) weeks, consisting of two supervised sessions and one unsupervised home session per week. Subjects: - 10-12 persons with an active diabetic foot ulcer - 2-3 kinesiologists Data collection: - Sociodemographic and health questionnaire (age, sex, gender, marital status, education level, employment status, average annual family income, medical and health history, pharmacological and non-pharmacological treatments); - Feasibility assessment: PA (physical activity) logbook including 1) the number of supervised and unsupervised sessions completed, 2) the duration of each session, 3) participation rate (number of patients recruited/number of eligible patients), 4) attrition rate (number of participants who completed the follow-ups/number of participants recruited), and 5) perceived facilitators and barriers; - Acceptability assessment: 1) Treatment Acceptability and Preference (TAP) Questionnaire, seven to nine additional questions to assess the use of provided material resources and required safety checks (capillary blood glucose and wound inspection) and collection of participants' feedback, and 2) Client Satisfaction Questionnaire (CSQ-8); - Assessment of the sensitivity of dependent variables to respond to the PA program*: 1) estimation of VO2max by a submaximal exercise test on a stationary bike (Aerobic Power Index submaximal exercise test), 2) average daily step count over seven days at the waist and in the offloading boot at times 0, 4, 8, and 12 weeks, 3) Global Physical Activity Questionnaire (GPAQ), 3) clinical examination (height, weight, body mass index, waist circumference, body fat percentage, blood pressure, resting heart rate, characteristics of the DFU and classification (SINBAD), 4) paraclinical examinations (venous blood glucose, glycated hemoglobin, lipid profile), 5) neuropathic pain questionnaire (DN4), 6) Epworth sleepiness scale, quality of life questionnaire (EQ-5D-5L), 7) questionnaire on motivation to practice PA. - Health and safety parameter measurements: electrocardiogram, oxygen saturation, estimated glomerular filtration rate, urine albumin/creatinine ratio, complete blood count. - Data collection at 24 and 36 weeks is also planned for participants who agree to be contacted after completing the 12-week PA program. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06092827
Study type Interventional
Source Université du Québec à Trois-Rivières
Contact Magali Brousseau-Foley, MD
Phone 819-372-5011
Email magali.brousseau-foley@uqtr.ca
Status Not yet recruiting
Phase N/A
Start date November 1, 2023
Completion date June 30, 2024

See also
  Status Clinical Trial Phase
Active, not recruiting NCT05659862 - Digitally Assisted Behavioral Physical Activity Intervention in Fibromyalgia N/A
Recruiting NCT05294692 - Using Behavioural Economics for More Sustainable Physical Activity mHealth Incentives: the Caterpillar App N/A
Recruiting NCT05619250 - Supervised Center-based vs. Unsupervised Home-based Exercise Programs (PRO-Training) N/A
Recruiting NCT06088485 - The Effect of Bone Mineral Density in Patients With Adult Cystic Fibrosis
Not yet recruiting NCT05963893 - Promoting a Healthy Life Through Gender Equity
Enrolling by invitation NCT05461989 - Physical Activity Barriers in Adolescent Hypertension Patients
Completed NCT06063187 - Technology-based Fall Risk Assessments for Older Adults in Low-income Settings
Active, not recruiting NCT06089876 - The Use of Mobile Applications in Obese and Overweight Adolescents for Health Improvement N/A
Recruiting NCT05608707 - APPETITE: Plant Protein and Exercise Solutions for the Prevention of Undernutrition in Older Adults. N/A
Enrolling by invitation NCT06033417 - Walking and Blood Pressure in Older Adults With Respiratory Impairment. N/A
Not yet recruiting NCT05887583 - Supporting Physical Literacy at School and Home N/A
Completed NCT05535400 - Effects of Physical-Psychological Integrative Intervention on SCI Patient: a Pilot Randomized Controlled Trial N/A
Recruiting NCT06095999 - Perfect Fit: Evaluation of a Virtual Coach for Smoking Cessation and Physical Activity N/A
Completed NCT06246812 - Text Message and Competition-Based Interventions Among University Students N/A
Recruiting NCT05935982 - Virtual Reality Exercise in a Community Highschool for Children With Disabilities Phase 1
Not yet recruiting NCT06027502 - Cardioprotective Benefit of Passive Heat Therapy in Higher-Level Spinal Cord Injury: Safety and Proof of Concept N/A
Recruiting NCT05147909 - Impact of Dietary Phosphate Excess on Exercise Capacity and Visceral Adiposity N/A
Recruiting NCT06185413 - Children's Cooperation Denmark: a 3-year System Dynamics Trial N/A
Completed NCT06018974 - Digital Gaming Intervention for Older People in Long-term Care N/A
Recruiting NCT05425641 - MoST-Influenced Behavioral Intervention for Walking Phase 2