Investigating the Related Factors and Outcome of Kinesiophobia and the Effects of Multidimensional Interventions in Cardiac Surgery Patients

Ai-Ling Chang

Status: Enrolling

Conditions: Cardiac Diseases Requiring Surgery

Treatments: Behavioral: the multidimensional interventions

Study type: Interventional

Funder types: Other

Identifiers

NCT06625892

231124

Details and patient eligibility

About

The primary objective of this two-year research project is to investigate the status of activity fear, its related factors, and prognosis in cardiac surgery patients in the first year. Subsequently, the study aims to develop a comprehensive intervention strategy combining exercise with cognitive-behavioral approaches tailored for cardiac surgery patients and assess the effectiveness of this intervention on activity fear, prognosis, and quality of life in the second year.

Full description

The study uses a convenient sampling method, focusing on patients undergoing cardiac surgery in the cardiac surgery ward of the Central Medical Center. The first-year research adopts a descriptive, correlational, and repeated-measures design, while the second-year research employs an experimental design. Participants are randomly assigned to either the experimental or control group. The experimental group undergoes a 12-week multidimensional interventions, while the control group receives no intervention. Data are collected through structured questionnaires. Data collection occurs at discharge, two weeks post-discharge, six weeks, 12 weeks, and 24 weeks.

Enrollment: 245 estimated patients

Sex: All

Ages: 18 to 100 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patients received cardiac surgery.
• Aged 18 or above.
• Clear consciousness and able to communicate in Mandarin or Taiwanese.
• Willing and consent to participate after being informed of the study purpose and procedures.

Exclusion criteria

• Cognitive impairment,
• Psychiatric disorders, and
• Long-term bedridden patients who rely on others for daily activities.

Trial design

Primary purpose: Supportive Care

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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245 participants in 2 patient groups

the interventions group

Experimental group

Description:

The experimental group undergoes a 12-week multidimensional interventions.

Treatment:

Behavioral: the multidimensional interventions

the control group

No Intervention group

Description:

the control group receives no intervention.