Effects of Adapted Snacktivity™ Intervention on Cognition and Self-Care in COPD Patients

1\. Background and Research Gaps: Chronic Obstructive Pulmonary Disease (COPD) is a severe global public health issue. In Hong Kong, COPD remains the second most common cause of respiratory hospitalisation, and 56% of COPD patients experience cognitive impairment (CI), which profoundly impacts patients' self-care abilities and quality of life. Despite a robust theoretical foundation, Snacktivity™ has not yet been validated for patients with COPD, and no randomised controlled trials have confirmed its efficacy in enhancing cognitive function and self-care abilities in this population. Two critical research gaps must be addressed: (1) the suitability of its current activity templates for COPD patients, and (2) the feasibility of its implementation in home and workplace settings. Nurses, physical therapists, occupational therapists, and caregivers offer complementary insights into practical challenges, patient-specific barriers, treatment adherence, and resource allocation requirements essential for tailoring the program to Hong Kong's contextual needs.

2 Study Objectives:

1. To explore the feasibility, acceptability, motivating factors, perceived barriers, and preferred formats of the culturally adapted Snacktivity™ program among COPD patients in Hong Kong, and to investigate stakeholders' perspectives, recommendations, and concerns regarding its implementation. 2. To examine the short-term and long-term effects of the culturally adapted Snacktivity™ program on patients' cognitive function and self-care abilities (primary outcomes), as well as on physical activity levels, self-efficacy, exercise capacity, health-related quality of life, anxiety, and depression (secondary outcomes). 3. To explore the overall efficacy and sustainable implementability of the culturally adapted Snacktivity™ program for COPD patients in Hong Kong.

3 Study Design: This is a three-phase sequential study.

1. Phase 1 (Co-design): Co-design workshops will be conducted with COPD patients (n=15), multidisciplinary healthcare professionals (nurses=6, physical therapists=6, occupational therapists=9), and family caregivers (n=6). The aim is to culturally adapt the Snacktivity™ program for Hong Kong COPD patients by gathering diverse perspectives on practical challenges, patient-specific barriers, treatment adherence, and preferred intervention formats. The co-design process follows a four-stage approach: Stage 1 (patient-only workshop), Stage 2 (multi-stakeholder workshop), Stage 3 (WhatsApp asynchronous feedback), and Stage 4 (patient final validation workshop). 2. Phase 2 (Feasibility Pilot RCT): A small-scale pilot randomised controlled trial will be conducted with 50 COPD patients (25 per group) to test the adapted program's feasibility and short-term clinical effects. The intervention lasts 12 weeks, with assessments at baseline and immediately post-intervention. Feasibility outcomes include recruitment and retention rates, intervention adherence, and dropout rates. This phase primarily evaluates feasibility outcomes to inform the design of the subsequent full-scale trial. Clinical outcomes measured in this phase include:

1. Cognitive function, assessed by the Hong Kong Montreal Cognitive Assessment (HK-MoCA) for global cognition, the Auditory Verbal Learning Test (AVLT) for memory, the Animal Fluency Test (AFT) for language, the Shape Trails Test (STT) for executive function, and the Digit Span Test (DST) for attention. 2. Self-care abilities, assessed by the Community COPD Self-Management Scale. 3. Physical activity levels, assessed by the Physical Activity Scale for the Elderly-Chinese version (PASE-C). 4. Self-efficacy, assessed by the Exercise Self-Regulatory Efficacy Scale-Chinese version (Ex-SRES-Chinese). 5. Exercise capacity, assessed by the 6-minute walk test (6MWT). 6. Health-related quality of life, assessed by the COPD Assessment Test (CAT). 7. Anxiety, assessed by the Generalised Anxiety Disorder-7 (GAD-7) scale. 8. Depression, assessed by the Patient Health Questionnaire-9 (PHQ-9) 3. Phase 3 (Full-scale RCT): A full-scale randomised controlled trial will be conducted with 160 COPD patients (80 per group) to evaluate the program's efficacy on the primary and secondary outcomes. The intervention duration and frequency remain consistent with Phase 2, but the content will be optimised based on Phase 2 findings. A 3-month post-intervention follow-up will be added to assess long-term effects. Assessments will occur at baseline, immediately post-intervention (Week 12), and 3 months post-intervention. This phase primarily evaluates clinical efficacy, with the same outcome measures and assessment tools as described in Phase 2.

4\. Hypotheses:

1. The culturally adapted Snacktivity™ program will demonstrate high feasibility among COPD patients in Hong Kong. 2. COPD patients participating in the culturally adapted Snacktivity™ program will show significant improvements in cognitive function and self-care abilities (primary outcomes), as well as in physical activity levels, self-efficacy, exercise capacity, health-related quality of life, and reductions in anxiety and depression (secondary outcomes), compared to the attention control group. 3. The culturally adapted Snacktivity™ intervention program will exhibit overall effectiveness and sustainable implementability among COPD patients in Hong Kong.

• Physical Activity Levels [Срок оценки: Baseline, immediately post-intervention (Week 12), and 3 months post-intervention (Phase 3 only)]
• Self-Efficacy [Срок оценки: Baseline, immediately post-intervention (Week 12), and 3 months post-intervention (Phase 3 only)]
• Exercise Capacity [Срок оценки: Baseline, immediately post-intervention (Week 12), and 3 months post-intervention (Phase 3 only)]
• Health-Related Quality of Life [Срок оценки: Baseline, immediately post-intervention (Week 12), and 3 months post-intervention (Phase 3 only)]
• Anxiety Symptoms [Срок оценки: Baseline, immediately post-intervention (Week 12), and 3 months post-intervention (Phase 3 only)]
• Depression Symptoms [Срок оценки: Baseline, immediately post-intervention (Week 12), and 3 months post-intervention (Phase 3 only)]