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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05403671
Other study ID # T0000/2022
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date September 1, 2022
Est. completion date May 31, 2024

Study information

Verified date May 2022
Source Turku University Hospital
Contact Maijastiina Rekunen
Phone +358504728980
Email maijastiina.rekunen@tyks.fi
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of the study is to increase the physical activity and exercise of those recovering from cancer (after treatments) and to promote a functional return to everyday life and coping in everyday life. The aim of the study is to evaluate the effects of a exercise intervention on the quality of life, functional fitness (functional muscle strength and endurance tests) and the amount of physical activity of the participants in the study.


Description:

Design: This is a quantitative study, whose data includes structured surveys (questionnaires) and measurements. Data are collected before and after the group exercise intervention. This 8 week tailored, progressive program will consist muscle strength training, endurance training, flexibility training, relaxation and home-exercises.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 50
Est. completion date May 31, 2024
Est. primary completion date May 31, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria: - Active cancer treatments have ended under 12 months - Age 18-70 years - Finnish speaking - moving without aids - z=1-0 - able to come Meri-Karina - normal or low physical activity - able to use digital equipments to participate remote exercise sessions Exclusion Criteria: - Exercise contraindications - Memory and mental health problems - Exercise every day over two hours

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Increasing Exercise and Physical Activity in Those Rehablilitating From Cancer
Intervention includes exercising and relaxation in a group

Locations

Country Name City State
Finland Maijastiina Rekunen Turku

Sponsors (2)

Lead Sponsor Collaborator
Turku University Hospital Lounais-Suomen Syöpäyhdistys

Country where clinical trial is conducted

Finland, 

Outcome

Type Measure Description Time frame Safety issue
Primary The change of Quality of life Eortec Qlqc-30 change from baseline at 8 weeks
Primary The change of Functional muscle strength upper and lower body functionals muscle strength tests change from baseline at 8 weeks
Primary The change of Endurance 6 min walking test change from baseline at 8 weeks
Primary The change of Subjective physical activity exercise diary change from baseline at 8 weeks
Primary The change of Subjective physical capability PROMIS-Cancer change from baseline at 8 weeks
Secondary Experiences and feedback subjective feedback survey only at 8 weeks
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