Intervention Effectiveness Towards Improving Physical and Mental Health for Post-stroke Patients.

Not Applicable

Completed

• Conditions: Brain Infarction; Cerebrovascular Disorders; Cerebral Infarction; Brain Ischemia; Stroke
• Interventions: Behavioral: Periodic health check program for post-stroke; Behavioral: Guiding the appropriate rehabilitation exercises; Behavioral: Motivational Interviewing; Device: Functional near-infrared spectroscopy

• Registration Number: NCT04941482
• Lead Sponsor: Hanoi Medical University

Brief Summary

This is a multi-intervention randomized controlled trial that aimed to develop a management pattern for stroke survivors. The program consists of monitoring the recovery process, early detecting the physical and mental disorders, suitably intervening for each patient to improve their quality of life. New intervention techniques will be firstly applied for post-stroke patients in Vietnam such as using the portable functional near-infrared spectroscopy (fNIRS) device to explore cortex frontal hemodynamic and motivational interviewing for psychological adjustment. A total of registered 92 stroke patients in Vietnam National Geriatrics Hospital will be included in the study for 6 months. Included patients will be randomized to an intervention group and received the long-term follow-up program or to a control group receiving standard care. The mental health and physical functioning of participants will be assessed at 0, 1, 3, and 6 months follow-up. This work was funded by Vingroup Joint Stock Company and supported by the Domestic Master/Ph.D. Scholarship Programme of Vingroup Innovation Foundation (VINIF), Vingroup Big Data Institute (VINBIGDATA).

Detailed Description

Stroke is a medical condition that occurs when a blood vessel that carries oxygen and nutrients to the brain is either blocked by a clot or bursts (or ruptures). This is a major cause of death and disability worldwide. Post-stroke patients will experience sudden and intense changes in their physical and mental health during the first year. Currently, there is no official management model for improving the physical and mental health of patients after stroke in Vietnam. Furthermore, traditional neuroimaging techniques such as Functional magnetic resonance imaging (fMRI), Positron emission tomography (PET), Electroencephalogram (EEG) are not suitable for routine monitoring due to limited flexibility dynamics and costs. Hence, this study aimed to develop a management pattern that includes monitoring the recovery process, early detecting the physical and mental disorders, suitably intervening for each patient to improve their quality of life. New intervention techniques will be firstly applied for post-stroke patients in Vietnam such as using the portable fNIRS device to explore cortex frontal hemodynamic and motivational interviewing for psychological adjustment. This randomized controlled trial study will include 92 post-stroke patients with dividing two groups (46 control \& 46 intervention subjects), who experience emergency by stroke within one week. A multi-intervention program will design for stroke patients including \[1\] periodic health examination for assessment of physical and mental health, recurrence risks, and harmful behaviors; \[2\] guiding the appropriate rehabilitation exercises for improving the physical status and monitoring through daily online report; \[3\] using the motivational interviewing methods to improve and prevent mental disorder; \[4\] applicating the technique of functional near-infrared spectroscopy (fNIRS) for measurement of oxy-hemoglobin on cortex prefrontal to early detect mental disorder and stroke recurrence risks. Outcome data will be collected via study questionnaires and fNIRS measuring results which are administered by researchers in the study site at 0, 1, 3, and 6 months follow-up. Simultaneously, Motivational Interviewing will carry out on post-stroke patients in the first three months (one time per week in the first month and one time per the second and third month). This intervention method aims to discover and resolve patient's conflicts by a standardized communication skill to improve their mental health and change negative behaviors. The scores of the Stroke Impact Scale (SIS), physical and mental assessment scales and fNIRS data in both the groups will be used to calculate the effect estimates of intervention methods with a measure of precision (95% CI) and assessed the results of the trial.

Study Timeline

• Study First Submitted: 2021-06-10
• Study First Submitted QC: 2021-06-21
• Study First Posted: 2021-06-28
• Study Start: 2021-08-01
• Status Verified: 2022-08
• Primary Completion: 2023-01-30
• Study Completion: 2023-06-30
• Last Update Submitted: 2024-02-27
• Last Update Posted: 2024-02-28

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 92

Inclusion Criteria

• Diagnosis of stroke according to WHO's definition of stroke
• Are managed at the National Geriatrics Hospital in Vietnam
• Include 24 hours to 1 week after stroke
• Provide informed consent
• Willing to attend intervention therapies & follow-up evaluations for half-year.
• Have conscious, cognitive, and communication abilities.

Exclusion Criteria

• Do not agree to participate in the study
• Are included in other experimental studies
• Have mental disorders before stroke attack
• Glasgow score ≤ 8
• Other diseases that make it difficult to complete the intervention

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Multi-intervention program	Periodic health check program for post-stroke	A multi-intervention program will design for stroke patients including \[1\] periodic health examination for assessment of physical and mental health, recurrence risks, and harmful behaviors; \[2\] guiding the appropriate rehabilitation exercises for improving the physical status and monitoring through daily online report; \[3\] using the motivational interviewing methods to improve and prevent mental disorder; \[4\] applicating the technique of functional near-infrared spectroscopy (fNIRS) for measurement of oxy-hemoglobin on cortex prefrontal to early detect mental disorder and stroke recurrence risks.
Multi-intervention program	Functional near-infrared spectroscopy	A multi-intervention program will design for stroke patients including \[1\] periodic health examination for assessment of physical and mental health, recurrence risks, and harmful behaviors; \[2\] guiding the appropriate rehabilitation exercises for improving the physical status and monitoring through daily online report; \[3\] using the motivational interviewing methods to improve and prevent mental disorder; \[4\] applicating the technique of functional near-infrared spectroscopy (fNIRS) for measurement of oxy-hemoglobin on cortex prefrontal to early detect mental disorder and stroke recurrence risks.
Standard care	Functional near-infrared spectroscopy	Standard health check and fNIRS measure
Multi-intervention program	Guiding the appropriate rehabilitation exercises	A multi-intervention program will design for stroke patients including \[1\] periodic health examination for assessment of physical and mental health, recurrence risks, and harmful behaviors; \[2\] guiding the appropriate rehabilitation exercises for improving the physical status and monitoring through daily online report; \[3\] using the motivational interviewing methods to improve and prevent mental disorder; \[4\] applicating the technique of functional near-infrared spectroscopy (fNIRS) for measurement of oxy-hemoglobin on cortex prefrontal to early detect mental disorder and stroke recurrence risks.
Standard care	Periodic health check program for post-stroke	Standard health check and fNIRS measure
Multi-intervention program	Motivational Interviewing	A multi-intervention program will design for stroke patients including \[1\] periodic health examination for assessment of physical and mental health, recurrence risks, and harmful behaviors; \[2\] guiding the appropriate rehabilitation exercises for improving the physical status and monitoring through daily online report; \[3\] using the motivational interviewing methods to improve and prevent mental disorder; \[4\] applicating the technique of functional near-infrared spectroscopy (fNIRS) for measurement of oxy-hemoglobin on cortex prefrontal to early detect mental disorder and stroke recurrence risks.

Primary Outcome Measures

Name	Time	Method
Changes from Baseline Mini-Mental State Examination (MMSE) at 1, 3, and 6 months	Baseline, 1, 3, and 6 month post intervention	A screening tool for post-stroke cognitive impairment. Scores range from 0 to 30 points, with lower scores indicating greater impairment. MMSE scores of approximately 21 to 25 are consistent with mild dementia, 11 to 20 with moderate, and 0 to 10 with severe.
Changes from Baseline Barthel Index (BI) at 1, 3, and 6 months	Baseline, 1, 3, and 6 months post intervention	Measure the changes of activities of daily living through assessing functional independence during half-year post-randomization. The score of the Barthel Index ranging from 0 to 100 was collected when 0 is the minimum (worst outcome) and 100 is the maximum (best outcome).
Changes from Baseline Stroke Impact Scale (SIS) at 1, 3, and 6 months	Baseline, 1, 3, and 6 months post intervention	Change from baseline to end-of-study (half-year post-randomization). Range: 0-100; positive values reflect an improvement.
Changes from Baseline Patient Health Questionnaire (PHQ-9) at 1, 3, and 6 months	Baseline, 1, 3, and 6 months post intervention	The Patient Health Questionnaire-9 (PHQ-9) is a screening tool for post-stroke depression and assessing the changes at baseline, 1, 3, and 6 months. The possible range is 0-27 and the higher scores mean worse outcomes (Depression Severity: 0-4 none, 5-9 mild, 10-14 moderate, 15-19 moderately severe, 20-27 severe)

Secondary Outcome Measures

Name	Time	Method
Fatigue severity scale (FSS)	Baseline, 1, 3, and 6 months post intervention	The fatigue severity scale (FSS) is a 9-item questionnaire with questions to measure fatigue for stroke patients. The items are scored on a 7 point scale from 1 (strongly disagree) to 7 (strongly agree). The minimum score = 9 and the maximum score possible =63. Higher the score is respectively greater fatigue severity.
Alcohol Use Disorders Identification Test-Concise (AUDIT-C)	Baseline, 1, 3, and 6 month post intervention	Alcohol Use Disorders Identification Test-Concise (AUDIT-C) is a 3-item alcohol screen that can help identify persons who are hazardous drinkers or have active alcohol use disorders. There are 3 questions and are scored on a scale of 0-12. Each question has 5 answer choices valued from 0 points to 4 points. In men, a score of 4 or more is considered positive, optimal for identifying hazardous drinking or active alcohol use disorders. In women, a score of 3 or more is considered positive.
Pittsburgh sleep quality index (PSQI)	Baseline, 1, 3, and 6 month post intervention	The Pittsburgh sleep quality index (PSQI) was designed as a self-rated questionnaire that assesses sleep quality and disturbances over a 1-month time. It includes seven subscores, each of which can range from 0 to 3. The subscores are tallied, yielding a total score that can range from 0 to 21. A total score of 5 or more indicates poor sleep quality; the higher the score, the worse the quality.
Fagerström Test for Nicotine Dependence (FTND)	Baseline, 1, 3, and 6 months post intervention	An ordinal measure of nicotine dependence related to cigarette smoking. In scoring the Fagerstrom Test for Nicotine Dependence, yes/no items are scored from 0 to 1 and multiple-choice items are scored from 0 to 3. The items are summed to yield a total score of 0-10. The higher the total Fagerström score, the more intense is the patient's physical dependence on nicotine.

Trial Locations

Locations (1)

National Geriatrics Hospital; 🇻🇳 Hanoi, Vietnam