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Clinical Trials in Singapore / NCT06596551
Unknown Not applicable

Aspirational Rehabilitation Coaching for Holistic Health (ARCH): A Pilot Pre-Post Experimental Study

NCT06596551 · tracked via the Priya Life Science Singapore tracker
Phase
Not applicable
Started
2024-03-01
Last updated
2024-09-19

Condition(s) studied

StrokePsychological Well-BeingPsychosocial Functioning

Investigational drug(s) / intervention(s)

Pre-Post ARCH Intervention

Pre-Post ARCH Intervention: Stroke dyads, consisting of a survivor and primary family caregiver, will engage in a 4 weekly, 1.5 hour experiential dyadic sessions, totalling 6 hours of participation. In Week 1, dyads acknowledge the losses occurring after the stroke to normalize feelings of grief and sadness and find comfort within the familial space. In Week 2, dyads interpret their post-stroke losses within the framework of their existing knowledge for managing adversities (strengths, resources, and values) and identify changes that are most meaningful to them. In Week 3, dyads set specific, measurable, and achievable goals to actualize the meaningful changes identified in Week 2. Finally in Week 4, dyads bring together their individually derived strengths from the previous sessions to culminate into strengthened dyadic bonds. The exercise will also encourage participants to expand beyond the dyadic space to seek support from their communities, social networks and care services that are available to them.

Study summary

The ARCH programme is a novel, strength-based, dyadic, multicomponent psychosocial intervention that blends together psychoeducation, psychosocial support and self-compassion practices to aid first-time stroke survivors and their family caregivers with their psycho-socio-emotional and spiritual challenges following discharge from in-patient care. A pre-post experimental design with a feasibility and acceptability assessment is adopted to evaluate and refine the ARCH intervention in promoting wellbeing, self-compassion, independence, quality of life, hope, resilience, self-efficacy and dyadic mutuality.

Eligibility

Sex
ALL
Min age
21 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: * Aged 21 years and above * Recovering from their first stroke at mild to moderate degree of severity * Discharged from inpatient care at no later than 3 months, * Clinically assessed to have cognitive capacities to engage in and complete the research study, * Language capabilities in English or Mandarin, and * One identified primary family caregiver aged 21 years and above with similar language capabilities. Exclusion Criteria: * Families with survivors suffering from aphasia, * Being too ill to participate, * Experiencing moderate to severe cognitive impairment, and * With family caregivers who are not interested to participate.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Tan Tock Seng Hospital Singapore Singapore Recruiting

More Nanyang Technological University trials in Singapore

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06596551 on ClinicalTrials.gov ↗ ← All trials in Singapore