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Completed

NCT Number: NCT02112955

A Self-efficacy Enhancing Stroke Self-management Program for Community-dwelling Stroke Survivors

The aim of this study is to examine the effectiveness of a nurse-led self-efficacy enhancing stroke self-management program on recovery of community-dwelling stroke survivors.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Acute public hospital 1, Kowloon, Hong Kong

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About this study

Previous systematic reviews showed that theory-based stroke self-management programs had potential benefits in improving stroke survivors' quality of life and self-efficacy. However there is a lack of evidence evaluating the effectiveness of a nurse-led theory-based stroke self-management program among community-dwelling Chinese stroke survivors.

This is a parallel group, single-blinded, randomized controlled trial to be held in a community center. All participants will be assessed at two time-points (baseline before randomization, and one month after program completion). Eligible participants will be randomly allocated to either the control group (receiving usual care) or the intervention group (receiving the self-efficacy enhancing stroke self-management program). Participants in the intervention group will receive an additional assessment on usefulness of the program immediately after program completion.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • aged 18 years or above
  • have a clinical diagnosis of stroke
  • currently live at home or will be discharged from hospital to home within one week
  • have a Mini Mental State Examination score >18
  • speak Cantonese
  • capable of giving informed consent
  • can attend sessions of the self-efficacy enhancing stroke self-management program
  • can use a phone

Exclusion criteria

  • diagnosed with transient ischemic attack, subdural or epidural hemorrhage
  • have cerebrovascular events due to presence of malignancy or head trauma
  • have limited comprehension and receptive aphasia
  • have been diagnosed with schizophrenia, bipolar disorder, or dementia
  • have received a stroke self-management program in the past 12 months as reported by the participants

Treatment and study plan

Stroke self-management program

Behavioral

A nurse-led community-based self-efficacy enhancing stroke self-management program.

Usual Care

Behavioral

Usual care such as hospital-based or community-based health education or services.

Primary outcomes

  1. Self-efficacy in performing stroke self-management behaviors

    Time frame: One month after the program

    Stroke Self-Efficacy Questionnaire

Secondary outcomes

  1. Stroke self-management behaviors

    Time frame: One month after the program

    Stroke Self-management Behaviors Performance Scale

  2. Health-related quality of life

    Time frame: One month after the program

    Stroke Specific Quality of Life Scale

  3. Depressive symptoms

    Time frame: One month after the program

    Geriatric Depression Scale

  4. Community reintegration

    Time frame: One month after the program

    Reintegration to Normal Living Index

  5. Outcome expectation

    Time frame: One month after the program

    Stroke Self-management Outcome Expectation Scale

Other outcomes

  1. Usefulness of the program

    Time frame: Within one week after the completion of the program

    Extent of overall program participation, and other qualitative comments.

Sponsors and collaborators

Lead sponsor

Queensland University of Technology

Other

Registry information

Official study title

A Randomized Controlled Trial of the Effectiveness of a Nurse-led Self-efficacy Enhancing Stroke Self-management Program for Community-dwelling Stroke Survivors

Acronym: SESSMP

Important dates

Study start
2014
Primary completion
2016
Study completion
2016
First posted
Apr 14, 2014
Registry last updated
Nov 9, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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