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Effects of a nurse-led supportive care programme for people with progressive neurological diseases on psycho-spiritual well-being

Effects of a nurse-led palliative care programme on psycho-spiritual well-being of patients with progressive neurological diseases : A mixed-method randomised controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300073090
Enrollment
Unknown
Registered
2023-06-30
Start date
2023-09-25
Completion date
Unknown
Last updated
2023-09-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

neurodegenerative diseases and neuromuscular diseases

Interventions

Group 1:Nurse-led psycho-spiritual intervention: Each session comprises two main parts. First, the therapist takes a supportive–expressive approach in encouraging the open expression of thoughts and e
Group 2:Befriending activity: The sessions will focus on discussion of neutral, everyday topics and events (e.g. hobbies, pets and current affairs) which are of interest to participants and are not la

Sponsors

The University of Hong Kong
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1. Are diagnosed with neurodegenerative disease including multiples sclerosis, Parkinson’s disease, and spinocerebellar ataxia or neuromuscular disease including motor neuron disease, muscular dystrophy, and spinal muscular atrophy; 2. Score >= 8 on the Hospital Anxiety and Depression Scale-Depression subscale (sensitivity and specificity of approximately 0.80); 3. Aged 18 or above; 4. Fluent Cantonese speaker; 5. Able to sign an informed consent form.

Exclusion criteria

Exclusion criteria: 1. Have severe cognitive impairment as indicated by the Abbreviated Mental Test lower than 6 (sensitivity and specificity of 0.94-0.96); 2. Are currently receiving psychotherapy/other behavioural interventions in the preceding six months; 3. Have prior experience in ACT-based intervention; 4. Have other contraindication or severe comorbidity that may limit their full participation (e.g. severe hearing or vision impairment).

Design outcomes

Primary

MeasureTime frame
psychological wellbeing;

Secondary

MeasureTime frame
spiritual wellbeing;meaning in life;symptom burden;psychological flexibility;distress and dying Distress scale;health-related quality of life;Illness representations;

Countries

China

Contacts

Public ContactLily Man Lee CHAN

The University of Hong Kong

cmlily@connect.hku.hk+852 3917 6329

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026