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N/A N=20 Randomized Double-blind Treatment

The Effects of Reaching Task Following Selective Trunk Stability Exercise

Cerebral Stroke · Hemiplegia, Spastic

Enrolled (actual)
20
Serious AEs
0.0%
Results posted
May 2025
Primary outcome: Primary: The Effect of a Particular Intervention During the Entire Course of the study_Trunk Dislocation — 304.97; 303.34 Millimeter — p=0.98

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Abdominal drawing-in maneuver exercise (Behavioral); sham (Behavioral)
Age
Adult, Older Adult · 40+ yrs
Sex
All
Sponsor
University of Valencia
Primary completion
Jul 2023

Outcome Measures

OutcomeResultp-value
PRIMARY
The Effect of a Particular Intervention During the Entire Course of the study_Trunk Dislocation
304.97; 303.34 0.98
PRIMARY
The Effect of a Particular Intervention During the Entire Course of the Study_movement Unit
4.30; 4.30 0.99
PRIMARY
The Effect of a Particular Intervention During the Entire Course of the Study_Elbow Angle
127.43; 134.13 0.68
SECONDARY
The Effect of a Particular Intervention During the Entire Course of the Study_Total Time
3.25; 3.06 0.56
SECONDARY
The Effect of a Particular Intervention During the Entire Course of the Study_Hand Velocity
684.13; 934.48 0.42
SECONDARY
The Effect of a Particular Intervention During the Entire Course of the Study_Elbow Angular Velocity
54.23; 41.98 0.45

Summary

This study is performed in a controlled randomized, two-period crossover design to test the efficacy of Abdominal drawing-in maneuver (ADIM) exercise compared to conventional physiotherapy in chronic stroke survivors.

Eligibility Criteria

Inclusion Criteria

  • The subject consisted of the physician's confirmation of chronic hemiplegia
  • onset ≥ 6 months
  • Mini-mental state examination≥25
  • Biceps ≤2, Triceps≤2
  • Ability to Sit on a chair alone
  • FMA UE score ≥ 21points, FMA UE≤ 60 points

Exclusion Criteria

  • Biceps>2, Triceps>2
  • Flaccid
  • Neglect syndrome
  • Have neurological disease and orthopedic disease
  • Lack of coordination
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT05767437). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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