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Enrolling by invitation NCT07018102

Nurse-Led Bedside Trunk Control Care Program

No phase Interventional Stroke

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Trunk Control Care Program.
Who it may be relevant to
Registry conditions: Stroke. Basic parameters: 20 years — 80 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Taiwan
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Nurse-Led Bedside Trunk Control Care Program for Patients With Stroke

Overview

This study aimed to apply care for stroke survivors by establishing trustable professional activities competency indicators and a trunk control care module for rehabilitation ward nurses during our second year.

Detailed description

Thus, the purposes of this study were: (1) to evaluate the effect of a stepwise nurse-led bedside trunk control care module intervention on improving trunk control, respiratory function, and quality of life in patients with stroke and (2) to modify and confirm the milestones and trustable professional activities of competence in trunk impairment care for patients with stroke to provide evidence-based nursing education and cultivate new nurses' competence in trunk injury care in the future.

Interventions

  • Other Trunk Control Care Program
    1. The intervention group underwent a 4-week bedside trunk control care module intervention based on routine care in a rehabilitation ward. 2. trunk control care module: combine the care strategies of "arm training, butterfly technique, shoulder control, diaphragmatic breathing" and "body awareness", practice twice a day, each time for 20-30 minutes, and can be adjusted according to the patient's condition.

Primary outcome measures

  • Trunk function [Time frame: Questionnaire were filled out three times, before the program intervention and at the two and fourth weeks following the intervention.]
Secondary outcome measures (4)
  • Postural control [Time frame: Questionnaire were filled out three times, before the program intervention and at the two and fourth weeks following the intervention.]
  • Respiratory function [Time frame: Questionnaire were filled out three times, before the program intervention and at the two and fourth weeks following the intervention.]
  • Body awareness [Time frame: Questionnaire were filled out three times, before the program intervention and at the two and fourth weeks following the intervention.]
  • stroke impact [Time frame: Questionnaire were filled out three times, before the program intervention and at the two and fourth weeks following the intervention.]

Eligibility criteria

Inclusion criteria

  • (a) Patients hospitalized for stroke in rehabilitation or neurology wards, currently in stable condition; (b) Trunk Impairment Scale score below 21; (c) aged 20 or above; (d) patients willing to participate.

Exclusion criteria

  • Patients with Trunk Impairment Scale score above 21, as this indicates that they can perform daily activities independently

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Supportive care

Study locations

Taiwan · 1 center
  • Chung Shan Medical University — Taichung

Identifiers

NCT: NCT07018102 · CS1-23077

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗