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Nineteen Years of Modified CIMT in a Clinical Setting, to Improve Arm and Hand Function After Stroke

NCT06671899 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 87

Last updated 2024-11-15

No results posted yet for this study

Summary

The goal of this observational study is to determine if clinically constraint-induced movement therapy (CIMT), when applied in a routine clinical practice, can improve arm- and hand function after stroke. Additionally, the study seeks to identify which patients experienced the greatest improvements, and to examine factors that contribute to the long-term sustainability of the treatment.

Stroke is one leading cause of disability, often resulting in difficulties using the arm and hand function on one side, making daily activities challenging. CIMT aims to enhance arm and hand function after stroke by incorporating intensive training and restraining the non-affected limb, thereby encouraging the use of the affected arm and hand. While numerous studies have demonstrated the effectiveness of CIMT, and it is recommended in national clinical guidelines, it is rarely implemented in clinical practice due to challenges in execution and sustainability. Moreover, it remains unclear which patients benefit the most from the treatment.

At a rehabilitation clinic in Sweden, CIMT has been incorporated into routine care for 19 years, which is uncommon. Participants undergo CIMT as outpatients over a three-week period, with one patient being treated at a time. By retrospectively observe outcomes from this clinically implemented and sustained model of CIMT, the study aims to address the following questions:

* Is CIMT, when conducted in a regular clinical setting, effective?
* Are there relationships between patient characteristics and outcomes?

Conditions

  • Stroke
  • Neurological Diseases or Conditions

Interventions

OTHER

Constraint-induced movement therapy (CIMT)

Clinically implemented modified CIMT. Including the three main components; intensive and repetitive task-oriented training of the affected limb, constraint of the non-affected limb and behavioural strategies known as the Transfer Package. In this model the training is supervised by therapist from several professions and some training sessions is performed in group settings with other inpatients and outpatients undergoing primary rehabilitation at the clinic.

Sponsors & Collaborators

  • Futurum - Academy for health and care

    collaborator UNKNOWN

  • Region Jönköping County

    lead OTHER_GOV

Principal Investigators

  • Kersti Samuelsson, Assoc.Prof. · Department of Health, Medicine and Caring Sciences, Linköping University, Linköping, Sweden

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2000-08-14
Primary Completion
2018-12-18
Completion
2018-12-18

Countries

  • Sweden

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06671899 on ClinicalTrials.gov