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Reborn Lifestyle Adjustment Program

A

Atlas University

Status

Enrolling

Conditions

Breast Cancer
Quality of Life

Treatments

Behavioral: Reborn lifestyle adjustment program
Procedure: Conventional Physiotherapy and Occupational Therapy

Study type

Observational

Funder types

Other

Identifiers

NCT06608043
E-22686390-050.99-46613

Details and patient eligibility

About

The aim of this study is to investigate the effects of the reborn lifestyle regulation program on physical activity, fatigue level, pain, mental health burden and quality of life in breast cancer patients.

Enrollment

60 estimated patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Being a female individual aged 18 or older
  • Have been diagnosed with Stage I, II, or III breast cancer
  • At least 6 months have passed since the completion of chemotherapy
  • Approval by an oncologist to participate in the study
  • Having internet access and the ability to connect online
  • Scoring above 23 on a standardized Mini Mental Status Examination Test
  • Being in the contemplation stage according to the Transtheoretical Model

Exclusion criteria

  • Having a neurological or systemic disease that could significantly affect the course of the intervention
  • Having metastasis that could impact the sustainability of the study
  • Suffering from neuropathic pain
  • Having participated in a healthy lifestyle program within the last 3 months

Trial design

60 participants in 2 patient groups

Intervention Group
Description:
This intervention group consists of multi-component modules developed to help individuals with breast cancer adopt a healthy lifestyle and improve their quality of life. The sessions are based on the 'Do Live Well' model, Kolb's Experiential Learning Theory, and CBT-based problem-solving skills.
Treatment:
Behavioral: Reborn lifestyle adjustment program
Control Group
Description:
Patients in the control group will continue conventional medical treatments, occupational therapy and physiotherapy sessions.
Treatment:
Procedure: Conventional Physiotherapy and Occupational Therapy

Trial contacts and locations

1

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Central trial contact

Sena Ondes, MSc

Data sourced from clinicaltrials.gov

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