Cancer SurvivorNCT05403671
Fit for Everyday Life - Increasing Exercise and Physical Activity in Those Rehablilitating From Cancer
A study testing Increasing Exercise and Physical Activity in Those Rehablilitating From Cancer in people with Cancer Survivor, run by Turku University Hospital at 1 site in Finland.
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. Read more about this study
- Who is it for?
- Ages 18 to 70 yearsHealthy volunteers can take part
- Conditions the study is for
- Cancer Survivor
- What is being tested?
- Increasing Exercise and Physical Activity in Those Rehablilitating From Cancer
- How many people
- 50 participants
- Where
- 1 siteFinland
- Study dates
- 1 Sep 2022to 31 May 2024
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 70 years
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Who may be able to join
- 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
Who cannot join
- Exercise contraindications
- Memory and mental health problems
- Exercise every day over two hours
Trial locations and contacts
1 site in 1 country.
Marianne Himberg contact
Finland1 site
Maijastiina Rekunen
Turku
Maijastiina Rekunen, MShealthcare, +358504728980, maijastiina.rekunen@tyks.fi
Marianne Himberg, MShealthcare, marianne.himberg@tyks.fi
About this study
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.
Read the detailed 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.
- Conditions
- Cancer Survivor
- Being tested
- Increasing Exercise and Physical Activity in Those Rehablilitating From Cancer
- Keywords
- exercise, cancer survivor, rehabilitation
- Medical subject headings
- Motor Activity
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Increasing Exercise and Physical Activity in Those Rehablilitating From CancerOther
Intervention includes exercising and relaxation in a group
What is being measured
The primary outcome is the main question the study is designed to answer.
The change of Quality of life
Eortec Qlqc-30
Measured: change from baseline at 8 weeks
The change of Functional muscle strength
upper and lower body functionals muscle strength tests
Measured: change from baseline at 8 weeks
The change of Endurance
6 min walking test
Measured: change from baseline at 8 weeks
The change of Subjective physical activity
exercise diary
Measured: change from baseline at 8 weeks
The change of Subjective physical capability
PROMIS-Cancer
Measured: change from baseline at 8 weeks
Secondary outcomes (1)
Experiences and feedback
subjective feedback survey
Measured: only at 8 weeks
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted3 Jun 2022
- Study start1 Sep 2022 (estimated)
- Primary completion31 May 2024 (estimated)
- Study completion31 May 2024 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Cancer SurvivorStudies of the same condition, open and under way.
- More trials run by Turku University HospitalThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Supportive care
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 50 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Turku University Hospital
- Sponsor type
- Other government
- Collaborators
- Lounais-Suomen Syöpäyhdistys
- Responsible party
- Sponsor
- Investigators
- Pia Vihinen, MD, PhD, Study director, Turku University Hospital
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05403671
- Sponsor's protocol ID
- T0000/2022
- Status last verified
- May 2022
- First submitted
- 10 May 2022
- Last updated
- 3 Jun 2022
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 3 Jun 2022. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Fit for Everyday Life - Increasing Exercise and Physical Activity in Those Rehablilitating From Cancer
- ClinicalTrials.gov ID
- NCT05403671
- Acronym / sponsor ID
- T0000/2022
- Conditions
- Cancer Survivor
- Keywords
- exercise, cancer survivor, rehabilitation
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 50 participants (estimated)
- Lead sponsor
- Turku University HospitalOther government
- Collaborators
- Lounais-Suomen Syöpäyhdistys
- Study start
- 1 Sep 2022 (estimated)
- Primary completion
- 31 May 2024 (estimated)
- Study completion
- 31 May 2024 (estimated)
- First posted
- 3 Jun 2022 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Detailed 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.
Study design
- Primary purpose
- Supportive care
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
Who may qualify
- Ages
- 18 to 70 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (8 listed)
- Active cancer treatments have ended under 12 months
- Age 18-70 years
- Finnish speaking
- moving without aids
- z=1-0
Key exclusion criteria (3 listed)
- Exercise contraindications
- Memory and mental health problems
- Exercise every day over two hours
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Increasing Exercise and Physical Activity in Those Rehablilitating From CancerIntervention includes exercising and relaxation in a group | Other | – |
Primary outcome
The change of Quality of life
Time frame: change from baseline at 8 weeks
Eortec Qlqc-30
The change of Functional muscle strength
Time frame: change from baseline at 8 weeks
upper and lower body functionals muscle strength tests
The change of Endurance
Time frame: change from baseline at 8 weeks
6 min walking test
The change of Subjective physical activity
Time frame: change from baseline at 8 weeks
exercise diary
The change of Subjective physical capability
Time frame: change from baseline at 8 weeks
PROMIS-Cancer
1 secondary outcome
Experiences and feedback
Time frame: only at 8 weeks
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 3 Jun 2022.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Marianne Himberg contact
Pia Vihinen, MD, PhD study director
Turku University Hospital
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Increasing Exercise and Physical Activity in Those Rehablilitating From Cancer in people with Cancer Survivor, run by Turku University Hospital at 1 site in Finland.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 8 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 3 Jun 2022. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Finland. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact Maijastiina Rekunen (+358504728980, maijastiina.rekunen@tyks.fi), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
The change of Quality of life (time frame: change from baseline at 8 weeks). The study lists 5 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 3 Jun 2022.