Construction and Preliminary Application of COM-B Based Sedentary Behavioural Booster Intervention Programme for Elderly Stroke Patients

Liu Shuxian

Status: Not yet enrolling

Conditions: Stroke

Treatments: Other: Sedentary behaviour intervention

Study type: Interventional

Funder types: Other

Identifiers

NCT06445868

HMUDQ20231116221

Details and patient eligibility

About

Explore the application effect of the sedentary behaviour intervention program for elderly stroke patients based on the COM-B model.

Full description

The goal of this clinical trial is to text about in the application effect of the sedentary behaviour intervention program for elderly stroke patients based on the COM-B model. The main question it aims to answer are:

• Changes in sedentary behaviour in elderly stroke patients Participants will received a 12-week sedentary behaviour intervention programme.

Researchers will compare differences in sedentary behaviour between routine care control and intervention groups.

Enrollment: 30 estimated patients

Sex: All

Ages: 60+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Meet the diagnostic criteria for cerebral infarction and cerebral hemorrhage in the Diagnostic Points for Various Major Cerebrovascular Diseases in China 2019 issued by the Cerebrovascular Disease Group of the Neurology Branch of the Chinese Medical Association;
• Age ≥60 years;
• National Institute of Health stroke scale (NIHSS) score <5 (i.e., mild stroke), stable vital signs, and able to cooperate with the survey;
• Total sedentary time ≥6 hours/day measured using the International Physical Activity Questionnaire;
• Resident for ≥6 months in the community residents;
• Patients or under the guidance of others can use WeChat.

Exclusion criteria

• Functional ambulation category scale (FAC) score <2;
• serious myocardial infarction, cerebral hemorrhage and pulmonary embolism in the acute stage of the need to limit the activities of the situation;
• is participating in other physical activity or sedentary behavioral intervention programs;
• severe muscle weakness, fractures and other diseases resulting in limited physical activity;
• serious mental disorders such as schizophrenia or dementia resulting in severe cognitive impairment;
• speech and communication disorders.

Trial design

Primary purpose: Supportive Care

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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30 participants in 2 patient groups

intervention group

Experimental group

Description:

Knowledge (information support, changing health attitudes); Motivation (motivation to change sedentary behaviour and improve exercise compliance); Capacity (development of exercise plans to improve sedentary behaviour change); Opportunities (increasing the timing of exercise and creating opportunities for sedentary behaviour change); Behaviour (monitoring and reinforcing sedentary behaviour change)

Treatment:

Other: Sedentary behaviour intervention

control group

No Intervention group

Description:

Routine nursing education