Stroke Clinical Trial
— NASTRUOfficial title:
A Randomized Controlled Trial of Nature-based Post-stroke Fatigue Rehabilitation (NASTRU)
| NCT number | NCT02435043 |
| Other study ID # | 2012/352 |
| Secondary ID | |
| Status | Completed |
| Phase | N/A |
| First received | |
| Last updated | |
| Start date | August 2012 |
| Est. completion date | January 2020 |
| Verified date | February 2020 |
| Source | Region Skane |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
The aim of NASTRU was to examine whether ten weeks of nature-based rehabilitation, as add-on to standard management, could influence post-stroke fatigue (primary outcome), depression, work ability or functional outcome (secondary outcomes), compared to controls.
| Status | Completed |
| Enrollment | 101 |
| Est. completion date | January 2020 |
| Est. primary completion date | May 2015 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 55 Years to 80 Years |
| Eligibility |
Inclusion Criteria: - Ischemic or haemorrhagic stroke - First ever or recurrence, about 3 months (group 1) or more than one year prior to screening (group 2) - Age: 55-80 years Exclusion criteria: - Dementia - Severe communication disorder that made it difficult to participate and/or serious illnesses besides stroke (for example, serious cancer disease) |
| Country | Name | City | State |
|---|---|---|---|
| Sweden | Skåne university hospital | Malmö |
| Lead Sponsor | Collaborator |
|---|---|
| Region Skane | Epidemiology and Register Centre South, Lund University, Swedish University of Agricultural Sciences |
Sweden,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Post stroke fatigue | Mental Fatigue Scale (MFS) pre-post design by blinded assessor. | 8 months after inclusion | |
| Primary | Occupational value of everyday occupation | Occupational Value (OVal-pd) pre-post design by blinded assessor | 8 months after inclusion |
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