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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03030092
Other study ID # Berg10069
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 2017
Est. completion date June 2019

Study information

Verified date July 2020
Source Molde University College
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

One group will receive today's standard rehabilitation program following hip fracture surgery. The intervention group will have maximal strength training incorporated in their program. It consists of 3 training sessions per week for 8 weeks, where 4-5 repetitions over 4 sets for leg press and abduction resistance exercise at ~85% of maximal strength is carried out. Muscle strength, balance and bone density will be compared between the groups following the 8-week rehabilitation period. The feasibility of the intervention for the patient group will be evaluated based on compliance with training program and possible adverse events related to the operated hip.


Recruitment information / eligibility

Status Completed
Enrollment 27
Est. completion date June 2019
Est. primary completion date June 2019
Accepts healthy volunteers No
Gender All
Age group 65 Years to 95 Years
Eligibility Inclusion Criteria:

- age over 65, hip fracture surgery

Exclusion Criteria:

- COPD, Heart failure, Dementia

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Maximal Strength Training
leg pres and abduction exercises

Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
Molde University College Central Norway Regional Health Authority

Outcome

Type Measure Description Time frame Safety issue
Primary Muscle strength 1RM leg press, and hip abduction 8 weeks
Primary Balance unipedal stance test 8 weeks
Primary Bone Density 8 weeks
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