Affective Responses in Neurological Rehabilitation

NCT ID: NCT02767466

Last Updated: 2016-05-10

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

16 participants

Study Classification

OBSERVATIONAL

Study Start Date

2012-12-31

Study Completion Date

2012-12-31

Brief Summary

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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.

Detailed Description

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Conditions

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Neurological Incidents Stroke Traumatic Brain Injury

Study Design

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Observational Model Type

CASE_CROSSOVER

Study Time Perspective

PROSPECTIVE

Study Groups

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G

All participants were randomly exposed to two different treatments:

* Conventional physical therapy (no specific device used)
* Robotic assisted gait training (Lokomat, Hocoma AG, Switzerland)

We consider the study as observational, since the both interventions of the study (physical therapy, robotic assisted gait training) did not change in the patients' usual therapy plan, as they received both interventions daily.

We only added diagnostic interventions to assess the affective responses.

Physical therapy and robotic assisted gait training

Intervention Type PROCEDURE

Interventions

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Physical therapy and robotic assisted gait training

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* voluntary participation
* neurological incident

Exclusion Criteria

* lack of communication ability
* interference of consciousness
* inability to speak German language
Minimum Eligible Age

18 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Universitaet Innsbruck

OTHER

Sponsor Role lead

Responsible Party

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Martin Burtscher

Prof Martin Burtscher

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Martin Kopp, Prof

Role: STUDY_DIRECTOR

Univeryity of Innsbruck

Other Identifiers

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APTRAGT001

Identifier Type: -

Identifier Source: org_study_id

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