NCT05403671

Brief 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.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
50

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Sep 2022

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

May 10, 2022

Completed
24 days until next milestone

First Posted

Study publicly available on registry

June 3, 2022

Completed
3 months until next milestone

Study Start

First participant enrolled

September 1, 2022

Completed
1.7 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 31, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 31, 2024

Completed
Last Updated

June 3, 2022

Status Verified

May 1, 2022

Enrollment Period

1.7 years

First QC Date

May 10, 2022

Last Update Submit

May 31, 2022

Conditions

Keywords

exercisecancer survivorrehabilitation

Outcome Measures

Primary Outcomes (5)

  • The change of Quality of life

    Eortec Qlqc-30

    change from baseline at 8 weeks

  • The change of Functional muscle strength

    upper and lower body functionals muscle strength tests

    change from baseline at 8 weeks

  • The change of Endurance

    6 min walking test

    change from baseline at 8 weeks

  • The change of Subjective physical activity

    exercise diary

    change from baseline at 8 weeks

  • The change of Subjective physical capability

    PROMIS-Cancer

    change from baseline at 8 weeks

Secondary Outcomes (1)

  • Experiences and feedback

    only at 8 weeks

Interventions

Intervention includes exercising and relaxation in a group

Eligibility Criteria

Age18 Years - 70 Years
Sexall(Gender-based eligibility)
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • 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

You may not qualify if:

  • Exercise contraindications
  • Memory and mental health problems
  • Exercise every day over two hours

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Maijastiina Rekunen

Turku, Finland

Location

MeSH Terms

Conditions

Motor Activity

Interventions

Exercise

Condition Hierarchy (Ancestors)

Behavior

Intervention Hierarchy (Ancestors)

Motor ActivityMovementMusculoskeletal Physiological PhenomenaMusculoskeletal and Neural Physiological Phenomena

Study Officials

  • Pia Vihinen, MD, PhD

    Turku University Hospital

    STUDY DIRECTOR

Central Study Contacts

Marianne Himberg

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
SUPPORTIVE CARE
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER GOV
Responsible Party
SPONSOR

Study Record Dates

First Submitted

May 10, 2022

First Posted

June 3, 2022

Study Start

September 1, 2022

Primary Completion

May 31, 2024

Study Completion

May 31, 2024

Last Updated

June 3, 2022

Record last verified: 2022-05

Data Sharing

IPD Sharing
Will not share

Locations