Distress improves after mindfulness training for progressive MS: A pilot randomised trial

Source: Bogosian et al. 2015 - Pubmed ID: 25767124

Setting: UK, Single center and Hospital

Study design:

RCT

 

Follow-up: 5 months

Patient group:

Sample size:
Total: 40 (36)
IG: 19 (17)
CG: 21 (19)

 

Inclusion criteria:

  • Multiple Sclerosis (PPMS or SPMS)
  • ≥3 on General Health Questionnaire (GHQ)-12
Type of technology:

Video consultations

Intervention:

Intervention: Intervention group were offered video-delivered (Skype) mindfulness once a week for eight weeks (8h sessions) in addition to usual care.

 

Duration: 8 weeks intervention and 3 months follow-up
Add on: +

 

Control group: Usual Care

Clinical effect/ Patient safety:

Clinical effect:

  • GHQ-12↓ (improved)
  • HADS↓ (improved)
  • MSIS-psychological and physical↓ (improved)
  • Pain↓ (improved)
  • Fatigue →

 

Patient safety: NA

Patient experiences/ Staff experiences:

Patient experiences: NA

 

Staff experiences: NA

Costs and organization:

Investment:
Equipment/Materials

  • Headset and webcam for patients

 

Running:
Staff Resources

  • Video-delivered Mindfulness

 

Organization: NA

 

Health care utilization:

  • QALY based on EQ-5D →
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Information

“↑”: Statistically significant increase

“↓”: Statistically significant decrease

“→”: Statistically insignificant (no difference)