Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03798418
Other study ID # CCH-170208
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 1, 2019
Est. completion date September 30, 2022

Study information

Verified date October 2022
Source Changhua Christian Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The objective of this study is to investigate the effects of therapeutic exercise and nutrition intervention for sarcopenia and risk of falls in patients with major chronic diseases. The outcomes will be analyzed regarding muscle strength, quality, and volume, etc., balance and gait, bone density, body composition, fall and quality of life after the intervention.


Description:

The main common chronic diseases in the elderly such as stroke, osteoporosis, chronic kidney disease and cancer, have been regarded as the fall high-risk patients. These patients are considered to be at risk for sarcopenia due to decreased exercise, nutritional status, and other reasons. Sarcopenia can be diagnosed and intervened effectively to delay the vicious cycle of health. Past studies have pointed out that in addition to drug intervention, treatment for sarcopenia must be accompanied by appropriate exercise and nutritional intervention (such as protein supplements, vitamin D) in order to achieve the best prevention and treatment.


Recruitment information / eligibility

Status Completed
Enrollment 186
Est. completion date September 30, 2022
Est. primary completion date September 30, 2022
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility - Inclusion Criteria: 1. 55-85 years old 2. 3-6 months after onset 3. walk independently for at least 10m - Exclusion Criteria: 1. lower limb Brunnstrom stage >5 2. combine other neuropathy diseases 3. significant deformity of lower limb include: Modified Ashworth scale(MAS) >3; contracture, fracture, chronic joint pain. 4. joint arthroplasty 5. unstable vital sign 6. can not cooperate study

Study Design


Intervention

Behavioral:
elastic band strengthening exercise
2-3days per week(150min per week)
Dietary Supplement:
diet counseling
each patients in this group will receive4-5times diet counseling

Locations

Country Name City State
Taiwan Changhua Christian Hospital Changhua

Sponsors (1)

Lead Sponsor Collaborator
Changhua Christian Hospital

Country where clinical trial is conducted

Taiwan, 

References & Publications (7)

Biolo G, Cederholm T, Muscaritoli M. Muscle contractile and metabolic dysfunction is a common feature of sarcopenia of aging and chronic diseases: from sarcopenic obesity to cachexia. Clin Nutr. 2014 Oct;33(5):737-48. doi: 10.1016/j.clnu.2014.03.007. Epub 2014 Mar 29. — View Citation

Cook WL, Tomlinson G, Donaldson M, Markowitz SN, Naglie G, Sobolev B, Jassal SV. Falls and fall-related injuries in older dialysis patients. Clin J Am Soc Nephrol. 2006 Nov;1(6):1197-204. Epub 2006 Aug 30. — View Citation

Couch ME, Dittus K, Toth MJ, Willis MS, Guttridge DC, George JR, Barnes CA, Gourin CG, Der-Torossian H. Cancer cachexia update in head and neck cancer: Definitions and diagnostic features. Head Neck. 2015 Apr;37(4):594-604. doi: 10.1002/hed.23599. Epub 2014 Mar 25. Review. — View Citation

Hyndman D, Ashburn A, Stack E. Fall events among people with stroke living in the community: circumstances of falls and characteristics of fallers. Arch Phys Med Rehabil. 2002 Feb;83(2):165-70. — View Citation

Kutner NG, Zhang R, Huang Y, Wasse H. Falls among hemodialysis patients: potential opportunities for prevention? Clin Kidney J. 2014 Jun;7(3):257-63. doi: 10.1093/ckj/sfu034. Epub 2014 Apr 15. — View Citation

Liu CJ, Latham NK. Progressive resistance strength training for improving physical function in older adults. Cochrane Database Syst Rev. 2009 Jul 8;(3):CD002759. doi: 10.1002/14651858.CD002759.pub2. Review. — View Citation

Stapleton T, Ashburn A, Stack E. A pilot study of attention deficits, balance control and falls in the subacute stage following stroke. Clin Rehabil. 2001 Aug;15(4):437-44. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Change of walking speed distance: 6m, patients can walk with foor orthosis and assistive devices baseline: before intervention; follow-up: 3 months after intervention
Primary Change of grip force Use a grip force meter (kg) to test both hands for test 3 times before intervention; follow-up: 3 months after intervention
Primary Change of postural sway displacement Use computerized dynography to measure the postural sway displacement (mm) before intervention; follow-up: 3 months after intervention
Primary Change of postural sway velocity Use computerized dynography to measure the postural sway velocity (mm/s) before intervention; follow-up: 3 months after intervention
Primary Change of postural sway area Use computerized dynography to measure the postural sway area (mm^2) before intervention; follow-up: 3 months after intervention
Primary Change of step time Use computerized dynography to measure spatial gait parameter: step time (ms) before intervention; follow-up: 3 months after intervention
Primary Change of stance time Use computerized dynography to measure spatial gait parameter: stance time (ms) before intervention; follow-up: 3 months after intervention
Primary Change of swing time Use computerized dynography to measure spatial gait parameter: swing time (ms) before intervention; follow-up: 3 months after intervention
Primary Change of single support time Use computerized dynography to measure spatial gait parameter: single support time (ms) before intervention; follow-up: 3 months after intervention
Primary Change of double support time Use computerized dynography to measure spatial gait parameter: double support time (ms) before intervention; follow-up: 3 months after intervention
Primary Change of step length Use computerized dynography to measure spatial gait parameter: step distance (mm) before intervention; follow-up: 3 months after intervention
Primary Change of stance length Use computerized dynography to measure spatial gait parameter: stance distance (mm) before intervention; follow-up: 3 months after intervention
Primary Change of muscle thickness Use ultrasound to assess muscles morphological parameter: thickness (mm). Target muscles include quadriceps, hamstring, anterior tibialis, gastrocnemius. before intervention; follow-up: 3 months after intervention
Primary Change of muscle fiber length Use ultrasound to assess muscles morphological parameter: fiber length (mm). Target muscles include quadriceps, hamstring, anterior tibialis, gastrocnemius. before intervention; follow-up: 3 months after intervention
Primary Change of muscle fiber orientation angle Use ultrasound to assess muscles morphological parameter: fiber orientation angle (degrees). Target muscles include quadriceps, hamstring, anterior tibialis, gastrocnemius. before intervention; follow-up: 3 months after intervention
Primary Change of muscle cross section area Use ultrasound to assess muscles morphological parameter: cross-sectional area (mm^2).
Target muscles include quadriceps, hamstring, anterior tibialis, gastrocnemius.
before intervention; follow-up: 3 months after intervention
Primary Change of physiological cost index (PCI) Heart rate (HR: beats/min) and walking speed (m/s) have been previously shown to be linearly related to oxygen uptake at sub-maximal exercise levels. Combination of these two parameters yields a single value in beats per meter, the physiological cost index (PCI). This is calculated as Working HR - Resting HR (beats/min) / Walking speed (m/s) before intervention; follow-up: 3 months after intervention
Primary Change of international Quality of Life Assessment Short Form -36 (SF-36) including 8 health concepts: (1) physical functioning, (2) role limitations because of physical health problems; (3) bodily pain, (4) social functioning, (5) general mental health (psychological distress and psychological wellbeing), (6) role limitations because of emotional problems, (7) vitality (energy/fatigue), (8) general health perceptions.
Scoring: answers to each question are scored which are then summed and transformed to a 0 - 100 scale.
The lower the score the more disability. The higher the score the less disability i.e., a score of zero is equivalent to maximum disability and a score of 100 is equivalent to no disability.
before intervention; follow-up: 3 months after intervention
Primary Change of amplitude of Muscle activity use electromyography to measure the muscles activity in microvolts (uv) included quadriceps, hamstrings, tibialis anterior, gastrocnemius during subject walking in self-selected speed in 6 meters. before intervention; follow-up: 3 months after intervention
Secondary Change of concentration of CRP (C-Reactive Protein) The concentration of CRP in the blood test. CRP is used mainly as a marker of inflammation. before intervention; follow-up: 3 months after intervention
Secondary Change of concentration of ALB (Serum albumin) The concentration of ALB in the blood test. Albumin is the most important contributor to the maintenance of plasma colloid oncotic pressure; deficiency results in edema. before intervention; follow-up: 3 months after intervention
Secondary Change of concentration of Glomerular Filtration Rate (GFR) The concentration of GFR in the blood test. The glomerular filtration rate is the best test to measure the patient's level of kidney function and determine the stage of kidney disease. It can calculate it from the results of the blood creatinine test. before intervention; follow-up: 3 months after intervention
Secondary Change of concentration of Hemoglobin (Hb) The concentration of Hb in the blood test. Time Frame: before intervention; follow-up: 3 months after intervention
Secondary Change of concentration of Glucose SPOT The concentration of Glucose SPOT in the blood test. TheSpot glucose measurement in epidermal interstitial fluid appears to be a promising alternative to capillary blood glucose estimation Time Frame: before intervention; follow-up: 3 months after intervention
Secondary Change of concentration of Cholesterol The concentration of Cholesterol in the blood test. before intervention; follow-up: 3 months after intervention
Secondary Change of concentration of Triglyceride The concentration of Triglyceride in the blood test. before intervention; follow-up: 3 months after intervention
Secondary Change of concentration of Transferrin The concentration of Transferrin in the blood test. before intervention; follow-up: 3 months after intervention
Secondary Change of Berg balance test (BBS) including 14 items which are scored on a 5 points scale (0-4). The degree of success in achieving each task is given a score of zero (unable) to four (independent), and the final measure is the sum of all of the scores.
The item scores are summed, minimum score =0, maximum score = 56
before intervention; follow-up: 3 months after intervention
Secondary Change of Fugl-Meyer Assessment (FMA) Items are scored on a 3-point ordinal scale (0 = cannot perform; 1 = performs partially; 2 = performs fully) Maximum Score = 226 points The 5 domains assessed include, Motor function (UE maximum score = 66; LE maximum score = 34), Sensory function (maximum score = 24), Balance (maximum score = 14), Joint range of motion (maximum score = 44), Joint pain (maximum score = 44) before intervention; follow-up: 3 months after intervention
Secondary Change of Body Mass Index (BMI) (body weight) kg/(height) m*(height)m before intervention; follow-up: 3 months after intervention
Secondary Change of Mini-mental state examination (MMSE) It is an 11-question measure that tests five areas of cognitive function:
orientation, registration, attention and calculation, recall, and language. The maximum score is 30. A score of 23 or lower is indicative of cognitive impairment.
before intervention; follow-up: 3 months after intervention
Secondary Change of Modified Ashworth scale (MAS) measures resistance during passive soft-tissue stretching, the score is ranged from 0-4 0: No increase in muscle tone
Slight increase in muscle tone, manifested by a catch and release or by minimal resistance at the end of the range of motion when the affected part(s) is moved in flexion or extension 1+: Slight increase in muscle tone, manifested by a catch, followed by minimal resistance throughout the remainder (less than half) of the ROM
More marked increase in muscle tone through most of the ROM, but affected part(s) easily moved
Considerable increase in muscle tone, passive movement difficult
Affected part(s) rigid in flexion or extension
before intervention; follow-up: 3 months after intervention
Secondary Change of Muscle tone measure the muscle tone (kg/m) under muscle resting. Target muscles are quadricep, hamstring, anterior tibialis, gastrocnemius. before intervention; follow-up: 3 months after intervention
See also
  Status Clinical Trial Phase
Recruiting NCT04043052 - Mobile Technologies and Post-stroke Depression N/A
Recruiting NCT03869138 - Alternative Therapies for Improving Physical Function in Individuals With Stroke N/A
Completed NCT04034069 - Effects of Priming Intermittent Theta Burst Stimulation on Upper Limb Motor Recovery After Stroke: A Randomized Controlled Trial N/A
Completed NCT04101695 - Hemodynamic Response of Anodal Transcranial Direct Current Stimulation Over the Cerebellar Hemisphere in Healthy Subjects N/A
Terminated NCT03052712 - Validation and Standardization of a Battery Evaluation of the Socio-emotional Functions in Various Neurological Pathologies N/A
Completed NCT00391378 - Cerebral Lesions and Outcome After Cardiac Surgery (CLOCS) N/A
Recruiting NCT06204744 - Home-based Arm and Hand Exercise Program for Stroke: A Multisite Trial N/A
Active, not recruiting NCT06043167 - Clinimetric Application of FOUR Scale as in Treatment and Rehabilitation of Patients With Acute Cerebral Injury
Enrolling by invitation NCT04535479 - Dry Needling for Spasticity in Stroke N/A
Completed NCT03985761 - Utilizing Gaming Mechanics to Optimize Telerehabilitation Adherence in Persons With Stroke N/A
Recruiting NCT00859885 - International PFO Consortium N/A
Recruiting NCT06034119 - Effects of Voluntary Adjustments During Walking in Participants Post-stroke N/A
Completed NCT03622411 - Tablet-based Aphasia Therapy in the Chronic Phase N/A
Completed NCT01662960 - Visual Feedback Therapy for Treating Individuals With Hemiparesis Following Stroke N/A
Recruiting NCT05854485 - Robot-Aided Assessment and Rehabilitation of Upper Extremity Function After Stroke N/A
Active, not recruiting NCT05520528 - Impact of Group Participation on Adults With Aphasia N/A
Active, not recruiting NCT03366129 - Blood-Brain Barrier Disruption in People With White Matter Hyperintensities Who Have Had a Stroke
Completed NCT05805748 - Serious Game Therapy in Neglect Patients N/A
Completed NCT03281590 - Stroke and Cerebrovascular Diseases Registry
Recruiting NCT05993221 - Deconstructing Post Stroke Hemiparesis