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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02915562
Other study ID # PMR-AGR-001
Secondary ID
Status Recruiting
Phase N/A
First received April 14, 2016
Last updated September 23, 2016
Start date April 2016

Study information

Verified date September 2016
Source Johannes Kepler University of Linz
Contact Christian Mittermaier, M.D.
Email christian.mittermaier@akh.linz.at
Is FDA regulated No
Health authority Austria: Ethikkommission
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine the effects of depressive mood on outcomes of an in-house rehabilitation program.


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date
Est. primary completion date October 2016
Accepts healthy volunteers No
Gender Both
Age group 60 Years and older
Eligibility Inclusion Criteria:

- 2-week in-house-rehab at an acute geriatric unit

- ability to take part in assessments

- understanding German language

- Informed Consent

Exclusion Criteria:

- anti-depressive medication shorter than 4 weeks before enrollment

- In-house rehab < 14 days

- advanced stage of dementia

Study Design

Allocation: Non-Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Basic Science


Related Conditions & MeSH terms


Intervention

Other:
exercise


Locations

Country Name City State
Austria Kepler University Hospital Linz

Sponsors (2)

Lead Sponsor Collaborator
Johannes Kepler University of Linz Kepler University Hospital

Country where clinical trial is conducted

Austria, 

Outcome

Type Measure Description Time frame Safety issue
Primary Physical Performance Test Change from baseline at day 14 +/-1 No
Primary de Morton Mobility Index The de Morton Mobility index is a method for measuring changes in mobility and enhancing the continuity of patient care across clinical settings Change from baseline at day 14 +/-1 No
Primary Performance Orientated Mobility Assessment (POMA) Task-oriented outcome measure that assesses gait and balance ability Change from baseline at day 14 +/-1 No
Primary Barthel Index The Barthel index is an ordinal scale used to measure performance in activities of daily living Change from baseline at day 14 +/-1 No
Primary Function Index Physiotherapy Change from baseline at day 14 +/-1 No
Primary Function Index Occupational Therapy Change from baseline at day 14 +/-1 No
Primary Grip strength measurement measured with JAMAR dynamometer Change from baseline at day 14 +/-1 No
Secondary Charlson Comorbidity Index Measure of comorbidity and multimorbidity Day 1+/-1 No
Secondary Timed Test of Money Counting Day 1+/-1 No
Secondary Geriatric Depression Scale (GDS-15) Day 1+/-1 and day 14+/-1 No