Delivery of a generic MBSR training to patients who visit a memory clinic with cognitive complaints, and who show no clinical signs of a cognitive disorder, is feasible.
ID
Bron
Aandoening
Mild cognitive impairment; cognitive complaints; memory complaints
[MCI; Cognitieve klachten; geheugenklachten]
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
Feasibility of delivering a generic MBSR training to patients who visit a memory clinic with cognitive complaints, and who show no clinical signs of a cognitive disorder
Achtergrond van het onderzoek
Rationale: Cognitive complaints of older individuals are often related to worries and concerns related to the ageing process and the associated change in cognitive functioning. Mindfulness-based interventions have been applied successfully to different clinical and non-clinical populations to relieve the burden of stress and ruminative thinking and to improve coping strategies in the context of physical and mental disease.
Objective: Is Mindfulness-based Stress Reduction (MBSR) feasible and effective in older persons with mild cognitive complaints?
Study design: Observational pilot study
Study population: N=10-12 patients of the Maastricht Memory Clinic in the age between 50 and 75 years; no diagnosis of cognitive disorder; no significant psychiatric comorbidity
Intervention (if applicable): Standard 8-week program of MBSR, comprising of 8 weekly group meetings of 2,5h and one silent retreat of 6h.
Main study parameters/endpoints: In this feasibility study, participants are interviewed after 8 weeks about their experiences during the training and how the training may be adjusted to fit the requirements for this target population even more in the future. Furthermore, the group effects of the training are evaluated by means of short questionnaires measuring life quality, mental health (perceived stress, anxiety and depressive symptoms), levels of mindfulness and self-compassion, and perceived burden of cognitive complaints, administered at baseline, 9 and 13 weeks. Feasibility of online cognitive assessment is tested at baseline and 9 weeks.
Nature and extent of the burden and risks associated with participation, benefit and group relatedness: MBSR training is nowadays widely available and can be safely followed without prior medical screening. Expectation of personal benefit from the training is realistic when the program is followed conscientiously, but cannot be guaranteed beforehand. Apart from the personal effort invested in participation and homework assignments, no adverse effects are to be expected.
Doel van het onderzoek
Delivery of a generic MBSR training to patients who visit a memory clinic with cognitive complaints, and who show no clinical signs of a cognitive disorder, is feasible.
Onderzoeksopzet
Week 0: interview, screening and assessment
Week 1-8: training
Week 9:assessment and interview
Week 13: 4-week follow-up assessment
Onderzoeksproduct en/of interventie
Custom 8-week Mindfulness-based Stress Reduction (MBSR)
Publiek
Maastricht University<br>
Po Box 616
Martin Boxtel, van
Maastricht 6200 MD
The Netherlands
+31 (0)43 3881041
martin.vanboxtel@maastrichtuniversity.nl
Wetenschappelijk
Maastricht University<br>
Po Box 616
Martin Boxtel, van
Maastricht 6200 MD
The Netherlands
+31 (0)43 3881041
martin.vanboxtel@maastrichtuniversity.nl
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
- Age between 50 and 75 years
- Existing complaints about at least one, or more aspects of cognitive functioning
- Expressed personal interest in participation in the training program
- Patients receive no further treatment for their complaint and will not revisit the memory clinic for a follow-up assessment for a period of at least 6 months
- Able to communicate in the Dutch language
- Availability on at least 7 of 8 (fixed) session dates
- Agreement to participate in homework assignments
- Home access to PC with internet connection (cognitive tests)
- Signed informed consent
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
- Clinical evidence of psychiatric comorbidity, or any psychotropic drug usage on a daily basis, which could interfere with participation in the group sessions and homework assignments
- Patients who receive (or will receive in a period of 4 months) medical treatment or psychological intervention of any kind for their cognitive condition
Opzet
Deelname
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In overige registers
Register | ID |
---|---|
NTR-new | NL4590 |
NTR-old | NTR4749 |
Ander register | NL49941.068.14 CCMO : METC 142043.3/ab |