Study protocol for a randomised controlled trial to determine the efficacy of an intensive seated postural intervention delivered with robotic and rigid trunk support systems

被引:3
作者
Santamaria, Victor [1 ]
Ai, Xupeng [2 ]
Chin, Karen [3 ,4 ]
Dutkowsky, Joseph P. [5 ]
Gordon, Andrew M. [3 ]
Agrawal, Sunil K. [2 ,6 ]
机构
[1] New York Med Coll, Dept Rehabil Sci, Phys Therapy Div, Valhalla, NY USA
[2] Columbia Univ, Mech Engn Dept, New York, NY 10027 USA
[3] Columbia Univ, Biobehav Sci Dept, New York, NY USA
[4] Burke Neurol Inst, White Plains, NY USA
[5] Columbia Univ, Dept Orthopaed Surg, New York, NY USA
[6] Columbia Univ, Dept Rehabil & Regenerat Med, New York, NY 10027 USA
来源
BMJ OPEN | 2023年 / 13卷 / 08期
基金
美国国家卫生研究院;
关键词
REHABILITATION MEDICINE; Paediatric neurology; Motor neurone disease; Clinical trials; GROSS MOTOR FUNCTION; OCCUPATIONAL PERFORMANCE-MEASURE; SEVERE CEREBRAL-PALSY; QUALITY-OF-LIFE; SEGMENTAL TRUNK; INTERNATIONAL CLASSIFICATION; ENVIRONMENT MEASURE; PAIN INTENSITY; CHILDREN; VALIDITY;
D O I
10.1136/bmjopen-2023-073166
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction Children with cerebral palsy (CP) classified as gross motor function classification system (GMFCS) levels III-IV demonstrate impaired sitting and reaching control abilities that hamper their overall functional performance. Yet, efficacious interventions for improving sitting-related activities are scarce. We recently designed a motor learning-based intervention delivered with a robotic Trunk-Support- Trainer (TruST-intervention), in which we apply force field technology to individualise sitting balance support. We propose a randomised controlled trial to test the efficacy of the motor intervention delivered with robotic TruST compared with a static trunk support system. Methods and analysis We will recruit 82 participants with CP, GMFCS III-IV, and aged 6-17 years. Randomisation using concealed allocation to either the TruST-support or static trunk-support intervention will be conducted using opaque-sealed envelopes prepared by someone unrelated to the study. We will apply an intention-to- treat protocol. The interventions will consist of 2 hours/sessions, 3/week, for 4 weeks. Participants will start both interventions with pelvic strapping. In the TruST-intervention, postural task progression will be implemented by a progressive increase of the force field boundaries and then by removing the pelvic straps. In the static trunk support-intervention, we will progressively lower the trunk support and remove pelvic strapping. Outcomes will be assessed at baseline, training midpoint, 1-week postintervention, and 3-month follow-up. Primary outcomes will include the modified functional reach test, a kinematic evaluation of sitting workspace, and the Box and Block test. Secondary outcomes will include The Segmental Assessment of Trunk Control test, Seated Postural & Reaching Control test, Gross Motor Function Measure-Item Set, Canadian Occupational Performance Outcome, The Participation and Environment Measure and Youth, and postural and reaching kinematics. Ethics and dissemination The study was approved by the Columbia University Institutional Review Board (AAAS7804). This study is funded by the National Institutes of Health (1R01HD101903-01) and is registered at clinicaltrials.gov. Trial registration number NCT04897347; clinicaltrials. gov.
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页数:12
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