Adolescent Idiopathic Scoliosis Clinical Trial
Official title:
Effects of Home Exercise Intervention on Bone Density, Muscle Functions, Quality of Life, and Curve Progression in Girls With Adolescent Idiopathic Scoliosis
Verified date | February 2020 |
Source | Chinese University of Hong Kong |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Studies with exercise intervention aimed to improve the bone health and muscle functions in patients with AIS were lacking. Evidence suggested that low bone mass and low muscle mass were associated with curve severity and occurrence of AIS. Weight-bearing exercise that aimed to improve musculoskeletal and metabolic health could enhance bone health and muscle mass, and could provide a feasible alternative conservative treatment to prevent curve progression as well as the quality of life in AIS girls. This is a pilot feasibility study for future large randomized controlled trial (RCT) aiming at determining the effects of home based exercise program on improving bone mineral density (BMD), muscle mass and functions, quality of life (QoL), and prevent curve progression in skeletally immature girls with adolescent idiopathic scoliosis (AIS).
Status | Completed |
Enrollment | 40 |
Est. completion date | August 20, 2019 |
Est. primary completion date | August 20, 2019 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 11 Years to 14 Years |
Eligibility |
Inclusion Criteria: - Cobb Angle greater or equal to 15° - Newly diagnosed at the Scoliosis Clinic without prior treatment - Cleared for physical activity by doctor Exclusion Criteria: - Scoliosis with any known etiology such as congenital scoliosis, neuromuscular scoliosis, scoliosis of metabolic etiology, scoliosis with skeletal dysplasia, or - Known endocrine and connective tissue abnormalities, or - Known heart condition or other diseases that could affect the safety of exercise - Eating disorders or GI malabsorption disorders or - Currently taking medication that affects bone or muscle metabolism |
Country | Name | City | State |
---|---|---|---|
Hong Kong | Prince of Wales Hospital | Shatin |
Lead Sponsor | Collaborator |
---|---|
Chinese University of Hong Kong |
Hong Kong,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Recruitment rate | The recruitment rate will be calculated based on the number of eligible subjects invited to the study and the number of eligible subjects agreed to participate. | 6 months | |
Other | Dropout rate | The dropout rates for the intervention and control groups will be calculated based on the number of recruited subjects in each group and the number of recruited subjects who failed to complete the 6-month exercise and complete all follow-up. | 6 months | |
Other | Dietary intake measures | Evaluation of habitual dietary intake will be based on retrospective means of assessment. A modified Food Frequency Questionnaire (FFQ) based on data obtained in the Hong Kong Adult Dietary Survey in 1995 will be used. The FFQ had been validated with the basal metabolic rate calculation and the 24-hour sodium/creatinine and potassium/creatinine analysis. Subjects will be asked about their usual frequency and consumption in the past twelve months from the food list. Standard portion size will be listed and a food photo album is provided to assist assessment. Any use of supplements will also be recorded. Daily nutrient intake is calculated by the Food Processor Nutrition analysis and Fitness software version 8.0 (Esha Research, Salem, USA), with addition of composition of some local foods based on food composition table from China. | Baseline, 6 months 18 months | |
Other | Physical activity measures | Physical activity level will be assessed with a physical activity bracelet and questionnaire. The subjects will be asked to wear the physical activity bracelet every day during the study period, thus provide an objective assessment of the physical activity of the wearer. Physical activity level of the subjects will also be assessed with the modified Baecke questionnaire adapted from Pols et al. | Baseline, 6 months 18 months | |
Other | Maturity assessment | Sexual maturity level including the breast development, onset of menarche, pubic hair distribution will be graded with standard Tanners Scale using the established and validated protocols. | Baseline, 6 months 18 months | |
Primary | Change in BMD after completion of exercise | Areal BMD (g/cm2) of non-dominant femoral neck and greater trochanter, and whole body BMD will be measured by DXA (Horizon, Hologic Inc., USA). Standardized scanning procedure provided by the manufacturer will be followed to ensure unified and comparable measurement. Quality assurance is performed by daily calibration against the standard phantoms provided by the manufacturer, with a precision error of 1.9% for BMD value for patient scan and <1.0% for whole body phantom scan. | Baseline and 6 months | |
Primary | Change in Muscle mass after completion of exercise | Muscle mass will be measurement by whole body less head (WBLH) scan with DXA (Horizon, Hologic Inc., USA). DXA is the current golden standard to the measurement of body composition. Standardized scanning procedure provided by the manufacturer will be followed to ensure unified and comparable measurement. | Baseline and 6 months | |
Primary | Change in Anthropometric measurements after completion of exercise | Body height, weight, sitting height, and arm span will be measured with standard stadiometry techniques. | Baseline and 6 months | |
Primary | Change in BMC after completion of exercise | BMC (g/cm) of non-dominant femoral neck and greater trochanter, and whole body BMC will be measured by DXA (Horizon, Hologic Inc., USA). Standardized scanning procedure provided by the manufacturer will be followed to ensure unified and comparable measurement. | Baseline and 6 months | |
Secondary | Change in clinical features after completion of exercise | A long standard standing postero-anterior (PA) whole spine radiograph will be used for grading curve severity in terms of Cobb angle according to the standard Cobb method. Risser sign, curve level and apex, and curve type will be recorded as in any standard assessment of scoliosis patients. | Baseline and 6 months | |
Secondary | Change in clinical features 1 year after completion of exercise | A long standard standing postero-anterior (PA) whole spine radiograph will be used for grading curve severity in terms of Cobb angle according to the standard Cobb method. Risser sign, curve level and apex, and curve type will be recorded as in any standard assessment of scoliosis patients. | Baseline and 18 months | |
Secondary | Change in muscle strength after completion of exercise | Legs, back, abdominal, and handgrip muscle strength will be assessed with dynamometer. The tests will be performed 3 times with 1 familiarization effort and 2 maximal effort, and the highest scores will be used for analysis. | Baseline and 6 months | |
Secondary | Change in muscle strength 1 year after completion of exercise | Legs, back, abdominal, and handgrip muscle strength will be assessed with dynamometer. The tests will be performed 3 times with 1 familiarization effort and 2 maximal effort, and the highest scores will be used for analysis. | Baseline and 18 months | |
Secondary | Change in muscle endurance after completion of exercise | Isometric squat test, Biering-Sorensen test, and isometric curl-up test will be used to assess the quadriceps, back and abdominal muscle endurance. The time (seconds) in which the subject maintained the position is recorded. | Baseline and 6 months | |
Secondary | Change in muscle endurance 1 year after completion of exercise | Isometric squat test, Biering-Sorensen test, and isometric curl-up test will be used to assess the quadriceps, back and abdominal muscle endurance. The time (seconds) in which the subject maintained the position is recorded. | Baseline and 18 months | |
Secondary | Change in aerobic fitness after completion of exercise | Aerobic fitness (estimated VO2max) of the subjects will be measured using sing-stage cycle ergometer sub-maximal test. Participants will be asked to sit on a cycle ergometer with 3-5 min warm up cycling at 150 kgm/min (25 Watt) workload, then workload will increase to 450-600 kgm/min (75-100 Watt) for another 6 minutes, in order to stimulate a submaximal exercise heart rate between 125-170 bpm. Estimated VO2max is then computed from the Astrand formula: VO2max = (workload x 2 + 300) * (200 - 73) / (exercise heart rate - 73)". Safety guidelines and procedures recommended by the ACSM will be followed. | Baseline and 6 months | |
Secondary | Change in aerobic fitness 1 year after completion of exercise | Aerobic fitness (estimated VO2max) of the subjects will be measured using sing-stage cycle ergometer sub-maximal test. Participants will be asked to sit on a cycle ergometer with 3-5 min warm up cycling at 150 kgm/min (25 Watt) workload, then workload will increase to 450-600 kgm/min (75-100 Watt) for another 6 minutes, in order to stimulate a submaximal exercise heart rate between 125-170 bpm. Estimated VO2max is then computed from the Astrand formula: VO2max = (workload x 2 + 300) * (200 - 73) / (exercise heart rate - 73)". Safety guidelines and procedures recommended by the ACSM will be followed. | Baseline and 18 months | |
Secondary | Change in quality of life after completion of exercise | The Quality of Life of the subjects will be assessed with the official Chinese version of Scoliosis Research Society-22 (SRS-22r) Questionnaire. SRS-22r is an internationally validated questionnaire that contains 22 questions organized in 5 domains covering different aspects of the quality of life of patients with scoliosis: function/activity, pain, self-image, mental health (5 items each), and satisfaction with treatment (2 items). | Baseline and 6 months | |
Secondary | Change in quality of life 1 year after completion of exercise | The Quality of Life of the subjects will be assessed with the official Chinese version of Scoliosis Research Society-22 (SRS-22r) Questionnaire. SRS-22r is an internationally validated questionnaire that contains 22 questions organized in 5 domains covering different aspects of the quality of life of patients with scoliosis: function/activity, pain, self-image, mental health (5 items each), and satisfaction with treatment (2 items). | Baseline and 18 months | |
Secondary | Change in BMD 1 year after completion of exercise | Areal BMD (g/cm2) of non-dominant femoral neck and greater trochanter, and whole body BMD will be measured by DXA (Horizon, Hologic Inc., USA). Standardized scanning procedure provided by the manufacturer will be followed to ensure unified and comparable measurement. Quality assurance is performed by daily calibration against the standard phantoms provided by the manufacturer, with a precision error of 1.9% for BMD value for patient scan and <1.0% for whole body phantom scan. | Baseline and 18 months | |
Secondary | Change in BMC 1 year after completion of exercise | BMC (g/cm) of non-dominant femoral neck and greater trochanter, and whole body BMC will be measured by DXA (Horizon, Hologic Inc., USA). Standardized scanning procedure provided by the manufacturer will be followed to ensure unified and comparable measurement. | Baseline and 18 months | |
Secondary | Change in muscle mass 1 year after completion of exercise | Muscle mass will be measurement by whole body less head (WBLH) scan with DXA (Horizon, Hologic Inc., USA). DXA is the current golden standard to the measurement of body composition. Standardized scanning procedure provided by the manufacturer will be followed to ensure unified and comparable measurement. | Baseline and 18 months | |
Secondary | Change in Anthropometric measurements 1 year after completion of exercise | Body height, weight, sitting height, and arm span will be measured with standard stadiometry techniques. | Baseline and 18 months |
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT03935295 -
Dysport ® as an Adjunctive Treatment to Bracing in the Management of Adolescent Idiopathic Scoliosis
|
Phase 4 | |
Recruiting |
NCT06262269 -
Interest of Adapted Physical Activity by Tele-rehabilitation in Chronic Pathology - Idiopathic Scoliosis in Adolescents
|
N/A | |
Not yet recruiting |
NCT06003010 -
Yoga for Adolescent Idiopathic Scoliosis (AIS) Patients
|
N/A | |
Withdrawn |
NCT02590380 -
Comparing Pedicle Screw Systems for the Treatment of Adolescent Paediatric Spine Deformity
|
N/A | |
Completed |
NCT02302534 -
Pilot Study of Functional and Morphometric Brain Abnormalities Related to Adolescent Idiopathic Scoliosis (MOR-FO-SIA)
|
N/A | |
Completed |
NCT05669859 -
Efficacy of Postoperative Telerehabilitation in Adolescent Idiopathic Scoliosis
|
N/A | |
Completed |
NCT05242601 -
Investigation of Quality of Life in Adolescent Idiopathic Scoliosis
|
||
Recruiting |
NCT05969301 -
Memory and Scoliosis Spinal Exercises
|
||
Recruiting |
NCT05919459 -
Effectiveness of Acceptance and Commitment Therapy Versus Active Controls in Improving Psychological Functions of Parents and Children With Adolescent Idiopathic Scoliosis: A Randomized Controlled Trial
|
N/A | |
Enrolling by invitation |
NCT05790031 -
Trials of Intelligent Nighttime Brace With Smart Padding to Treat of Adolescent Idiopathic Scoliosis
|
N/A | |
Active, not recruiting |
NCT04867148 -
The Prediction and Prevention of Disease by Using Big Data in Motion Analysis
|
N/A | |
Completed |
NCT05056363 -
The Effects of Core Stability Training in Children With Adolescent Idiopathic Scoliosis
|
N/A | |
Completed |
NCT00989495 -
Comprehensive Cohort Study of Bracing for Adolescent Idiopathic Scoliosis (AIS): A Feasibility Study
|
N/A | |
Withdrawn |
NCT00958373 -
Risk Factors for Psychiatric Disorders Associated With Adolescent Idiopathic Scoliosis
|
N/A | |
Recruiting |
NCT05730920 -
IV Methadone vs EXPAREL Erector Spinae Plane Blockade in Pediatric Subjects Undergoing Idiopathic Scoliosis Correction
|
Phase 4 | |
Recruiting |
NCT03292601 -
Brace Monitoring for Adolescent Idiopathic Scoliosis (AIS)
|
N/A | |
Completed |
NCT04421157 -
Exercises in Adolescent Idiopathic Scoliosis
|
N/A | |
Completed |
NCT05127902 -
Association Between Postural Balance and Muscle Activity of the Lumbar and Lower Limb Muscles in Female With or Without Adolescent Idiopathic Scoliosis (AIS) During Standing Balance Tasks With Upper Limb Movement
|
||
Completed |
NCT05703737 -
Respiratory Function and Respiratory Muscle Strength in Adolescent Idiopathic Scoliosis
|
||
Completed |
NCT04092335 -
Evaluation of Adam's Forward Bend Test and Smartphone Application in Screening of Adolescent Idiopathic Scoliosis
|