Fit for Everyday Life - Increasing Exercise and Physical Activity in Those Rehablilitating From Cancer

NCT ID: NCT05403671

Last Updated: 2022-06-03

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

50 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-09-01

Study Completion Date

2024-05-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

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

See the medical conditions and disease areas that this research is targeting or investigating.

Cancer Survivor

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

NONE

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Increasing Exercise and Physical Activity in Those Rehablilitating From Cancer

Intervention includes exercising and relaxation in a group

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

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
Minimum Eligible Age

18 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Lounais-Suomen Syöpäyhdistys

UNKNOWN

Sponsor Role collaborator

Turku University Hospital

OTHER_GOV

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Pia Vihinen, MD, PhD

Role: STUDY_DIRECTOR

Turku University Hospital

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Maijastiina Rekunen

Turku, , Finland

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Finland

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Maijastiina Rekunen

Role: CONTACT

+358504728980

Marianne Himberg

Role: CONTACT

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

Maijastiina Rekunen, MShealthcare

Role: primary

+358504728980

Marianne Himberg, MShealthcare

Role: backup

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

T0000/2022

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Rehabilitation - Physical Activity and Coping
NCT04245943 ACTIVE_NOT_RECRUITING NA
Fit to Fight Childhood Cancer
NCT05867186 RECRUITING
Effectiveness of a Cancer Exercise Program
NCT06039488 ENROLLING_BY_INVITATION NA