Skip to content

Does early targeted trunk training improve mobility outcome at 6 months for patients who are unable to sit unsupported at admission?

Additional Trunk Training in Early Stroke Trial (ATTEST): A mixed method feasibility study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN12137158
Enrollment
20
Registered
2015-12-23
Start date
2016-02-01
Completion date
Unknown
Last updated
2016-10-17

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

Conditions

Topic: Stroke

Interventions

The patient will receive a minimum of 16 hours of additional trunk training over a 6-8 week period, focussing on strengthening and functional exercises. Specific trunk strength training exercises wil

Sponsors

King's College London
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria (updated on 19/09/2016): 1. Aged 18 years or over 2. Between day 3 and day 7 of a supra tentorial lesion associated with an ischaemic or haemorrhagic stroke 3. With hemiparesis involving the arm and leg 4. Able to understand and follow a one-stage command 5. With significant trunk deficit evidenced by an inability to sit independently for 30 seconds 6. Able to provide informed consent in accordance with the Mental Capacity Act (2005) 7. Patients with mild aphasia can be included, the consent procedure will be facilitated using pictorial aphasia-friendly participant information booklets and communication other than spoken language (for example, gestures, strategic use of environmental cues) in line with Connect recommendations 8. Non-English speakers will be included if the aid of an interpreter is available via the NHS Sub-study: 1. Those meeting inclusion criteria (above) 2. Lacking mental capacity to give informed consent Original inclusion criteria: 1. Aged 18 years or over 2. Between day 3 and day 7 of a first supra tentorial lesion associated with an ischaemic or haemorrhagic stroke 3. With hemiparesis involving the arm and leg 4. Able to understand and follow a two-stage command 5. With significant trunk deficit evidenced by an inability to sit independently for 30 seconds 6. Able to provide informed consent in accordance with the Mental Capacity Act (2005) 7. Patients with mild aphasia can be included, the consent procedure will be facilitated using pictorial aphasia-friendly participant information booklets and communication other than spoken language (for example, gestures, strategic use of environmental cues) in line with Connect recommendations 8. Non-English speakers will be included if the aid of an interpreter is available via the NHS

Exclusion criteria

Exclusion criteria: Exclusion criteria (updated on 19/09/2016): 1. Individuals with brainstem or cerebellar strokes associated with severe symptoms of dizziness or positional vertigo exacerbated by exercise. Screening for severe dizziness will be ascertained by the medical staff before recruiting. 2. Clinically significant pre-morbid levels of disability 3. Not medically stable as defined by the medical team Original exclusion criteria: 1. Individuals with brain stem, cerebellar or multiple stroke lesion 2. Previous neurological disease affecting motor performance 3. Not medically stable

Design outcomes

Primary

MeasureTime frame
Feasibility measures of recruitment, retention and attrition will be determined through screening and completion data to measure the number of admitted patients that fulfil the study inclusion/exclusion criteria; consent to take part in the study; complete the trunk training intervention; and complete baseline, post intervention and 6 month follow up assessments of the secondary outcome measures.

Secondary

MeasureTime frame
1. Trunk impairment is measured using the Trunk Impairment Scale at baseline, post intervention and at 6 months follow-up 2. Mobility is measured using the Modified Rivermead Mobility Index at baseline, post intervention and at 6 months follow-up 3. Quality of life is measured using the Stroke Specific Quality of Life Scale and SF-6D at baseline, post intervention and at 6 months follow-up 4. Quality of life and health costs (QALYs) are measured using the EQ5D-5L at baseline, post intervention and at 6 months follow-up

Countries

United Kingdom

Outcome results

None listed

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