Affective Responses in Neurological Rehabilitation

Stroke Clinical Trial

Official title:

A Preliminary Study on Acute Affective Responses Focussing on Differences Between Physical Therapy and Robotic Assisted Gait Training

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02767466
• Other study ID #: APTRAGT001
• Status: Completed
• Phase: N/A
• First received: April 22, 2016
• Last updated: May 9, 2016
• Start date: December 2012
• Est. completion date: December 2012

Study information

• Verified date: May 2016
• Source: Universitaet Innsbruck
• Contact: n/a
• Is FDA regulated: No
• Health authority: Austria: Ethikkommission
• Study type: Observational

Clinical Trial Summary

Using a single blind within-subject design, 16 patients with neurological disorders were randomly exposed to two different treatments: physical therapy and robotic assisted gait training. Both before and after the treatments, a self-report Mood Survey Scale (MSS) was used to assess the effects on the treatment on distinct affective states. The subscales of the MSS were tested for pre-post changes and different effects between treatments with non-parametric tests.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 16
• Est. completion date: December 2012
• Est. primary completion date: December 2012
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 80 Years

Eligibility

Inclusion Criteria:

• voluntary participation

• neurological incident

Exclusion Criteria:

• lack of communication ability

• interference of consciousness

• inability to speak German language

Study Design

Observational Model: Case-Crossover, Time Perspective: Prospective

Related Conditions & MeSH terms

• Neurological Incidents
• Stroke
• Traumatic Brain Injury

Intervention

Procedure:
• Physical therapy and robotic assisted gait training

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Universitaet Innsbruck

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change of subscales of mood survey scale from pre to post treatment		30-60 minutes	No