Skip to content

Postural Control Training in Type II Spinal Muscular Atrophy: Protocol for a Randomized Controlled Trial

Postural Control Training in Type II Spinal Muscular Atrophy: Protocol for a Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600118427
Enrollment
Unknown
Registered
2026-02-05
Start date
2026-05-08
Completion date
Unknown
Last updated
2026-02-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Spinal Muscular Atrophy type ?

Interventions

Experimental Group:Trunk Control Exercise
Control Group:Home-based Guidance

Sponsors

West China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
3 Years to 17 Years

Inclusion criteria

Inclusion criteria: Inclusion Criteria for SMA Study Participants: Participants must (1) be diagnosed with SMA type II by a neurologist and confirmed through genetic testing; (2) be aged 3–17 years and score =27 on the Mini-Mental State Examination (MMSE) to ensure adequate cognitive ability to comprehend and cooperate with the study; (3) demonstrate the ability to maintain sitting balance independently or with minimal assistance (meeting Bobath Sitting Balance Grade I or lower); (4) be receiving ongoing treatment with Nusinersen to maintain consistency in clinical management; (5) attend outpatient physical therapy sessions at least three times per week; and (6) provide written informed consent from either the participant or their legal guardian following full comprehension of the study details.

Exclusion criteria

Exclusion criteria: Participants will be excluded if they: (1) have previously undergone spinal surgery requiring extended bedside care; (2) are currently enrolled in other SMA-related rehabilitation programs at hospitals, clinics, or rehabilitation centers; (3) present with conditions unsuitable for rehabilitation exercises, such as pain during movement, post-exercise injuries, or strains; (4) are unable to provide informed consent, either personally or through a legal guardian; (5) can only attend fewer than five therapy sessions per week for any reason; or (6) are unable to complete the study due to fatigue or muscle weakness.

Design outcomes

Primary

MeasureTime frame
Functional near-infrared brain imaging status, fNIRS;Surface electromyographic (sEMG) activation status of the targeted muscle group(s);

Secondary

MeasureTime frame
Hammersmith functional motor scale Expanded,HFMSE;ratings of perceived exertion,RPE;Pediatric Quality of Life Inventory Multi Dimensional Fatigue Score,PedsQLMFS;

Countries

China

Contacts

Public ContactZhang Jing

West China Hospital of Sichuan University

252482329@qq.com+86 151 0849 1709

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 15, 2026