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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02702557
Other study ID # 2016-42
Secondary ID
Status Completed
Phase N/A
First received February 29, 2016
Last updated May 2, 2016
Start date February 2016
Est. completion date May 2016

Study information

Verified date May 2016
Source Aalborg Universitetshospital
Contact n/a
Is FDA regulated No
Health authority Denmark: Ethics Committee
Study type Interventional

Clinical Trial Summary

This feasibility study investigates if frail elderly and hospitalized patients are able to perform unsupervised elastic band exercises as a supplement to their usual supervised physiotherapy sessions and how much training they perform during their hospitalization. It is also investigated how the frail elderly and the health personnel experiences the unsupervised elastic band exercises.


Recruitment information / eligibility

Status Completed
Enrollment 15
Est. completion date May 2016
Est. primary completion date April 2016
Accepts healthy volunteers No
Gender Both
Age group 65 Years and older
Eligibility Inclusion Criteria:

- Frail elderly and hospitalized patients with a minimal score of 5/15 measured by the Tilburg Frailty Indicator

- Able to read and understand Danish

Exclusion Criteria:

- Frail elderly and hospitalized patients with a score of <5 measured by the Short Portable Mental Status Questionnaire

- Frail elderly and hospitalized patients where resistance training and physical activity is contraindicated (evaluated by a geriatrician and/or physiotherapist)

Study Design

Intervention Model: Single Group Assignment, Masking: Open Label


Related Conditions & MeSH terms


Intervention

Other:
Elastic Band Exercises


Locations

Country Name City State
Denmark Aalborg University Hospital Aalborg North Region Denmark

Sponsors (5)

Lead Sponsor Collaborator
Aalborg Universitetshospital Aalborg University, Amager Hospital, Hvidovre University Hospital, University of Copenhagen

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Other Mean deviation from the prescribed TUT per repetition in seconds during the course of the intervention The mean deviation is calculated as the difference between actual TUT and prescribed TUT (8 seconds). From inclusion-discharge from hospital - up to 6 weeks No
Other Difference in score of two tests: The 30-s chair stand and the de Morton Mobility Index (DEMMI) From beginning of hospitalization to discharge from hospital - up to 6 weeks No
Primary Total number of sets performed From inclusion-discharge from hospital - up to 6 weeks No
Secondary The total number of repetitions performed From inclusion-discharge from hospital - up to 6 weeks No
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