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The implementation of the Dutch Serial Trial Intervention (STA OP!).

The implementation of the serial trial intervention for pain and challenging behavior in advanced dementia patients in Dutch nursing homes, "STA OP!".

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON26483
Enrollment
168
Registered
2009-08-26
Start date
2009-09-01
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

Dementia-patients (Reisberg GDS, 5, 6 or 7) with symptoms of pain and/or challenging behavior (measured with MDS-pain, PACSLAC-D, NPI-NH and CMAI).

Interventions

In 5 meetings of 4 hrs each, nurses and nursing home physicians of all experimental wards are trained in the use of the steps in the protocol. The training is given by two collaborating, experienced t
2. The SECOND step is to perform a needs assessment that focuses on affective needs of people with dementia
3. The THIRD step concerns a trial of non-pharmacological comfort interventions
4. The FOURTH step is a trial of analgesics
5. STEP FIVE refers to consultation of other health care professionals or practitioners, or a trial of psychotropic drugs.

Sponsors

- VU University Medical Center (Department of Nursing home medicine) - EMGO+ Institute of Health and Care Research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Global Detoriation Scale (Reisberg 1983), (GDS) > 5; 2. No chronic psychiatric diagnosis other than dementia; 3. CMAI > 44, NPI > 4, MDS-pain = pain. In all included residents: 1. PACSLAC-D (pain observations); 2. Depression (Cornell and MDS-depression); 3. Quality of Life (Qualidem); 4. ADL (Katz); 5. Co-morbidity (ICD-10); 6. Demographics; 7. Apo-E4 (Buccal mucosa swab).

Exclusion criteria

Exclusion criteria: 1. GDS-score < 5; 2. Chronic psychiatric diagnosis other than dementia.

Design outcomes

Primary

MeasureTime frame
Pain: measured with painscale of the Dutch version of the MDS-RAI and PACSLAC-D Behavior: CMAI, NPI-NH.

Secondary

MeasureTime frame
1. Depression: Cornell-depression and MDS-DRS; 2. Quality of Life: Qualidem; 3. Use of anti-psychotic medication.

Contacts

Public ContactM.J.C. Pieper

Department of Nursing home medicine and the EMGO Institute for Health and Care Research, VU University Medical Center Amsterdam van der Boechorststraat 7, Room B-544

m.pieper@vumc.nl+31(0)20 444 9366

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)