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Completed

NCT Number: NCT01495650

Effect of a Tailored Program of Physical Activity and Nutritional Counseling on Fatigue Reduction in Breast Cancer Patients Receiving an Adjuvant Treatment

Cancer-related fatigue is by far the most common symptom affecting cancer patients. Combining regular dietary counseling and tailored physical activity is associated with reduced cancer-related fatigue and can improve quality of life and body weight control. We propose to conduct a randomized controlled trial which purpose is to evaluate the effect of an intervention combining physical exercise and nutritional therapeutic education on cancer-related fatigue. To gain behavioral change towards PA and nutrition habits, interventions will take place within hospitals, on the same days of adjuvant treatments.

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Key information

Age range

18 year–76 year

Sex eligibility

Female

Study type

Interventional

Phase

Phase 3

Primary location

CRLC Val d'Aurelle-Paul Lamarque

Montpellier, 34298, France

About this study

Cancer-related fatigue is by far the most common symptom affecting cancer patients. Combining regular dietary counseling and tailored physical activity is associated with reduced cancer-related fatigue and can improve quality of life and body weight control. We propose to conduct a randomized controlled trial which purpose is to evaluate the effect of an intervention combining physical exercise and nutritional therapeutic education on cancer-related fatigue. To gain behavioral change towards PA and nutrition habits, interventions will take place within hospitals, on the same days of adjuvant treatments.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Female patient with histologically proven breast cancer
  • 18-76 years old
  • Patients having undergone curative surgery and eligible to 6 cycles of adjuvant chemotherapy (6 FEC100, or 3FEC100 + taxanes) followed by radiotherapy
  • Satisfactory healing of breast and lymph nodes area
  • Ability to understand the nature, goal and study methodology
  • Consent to cooperate for clinical assessments
  • Affiliation to a social security regime or beneficiary of equivalent social protection
  • Written informed consent provided before any study specific procedures

Exclusion criteria

  • HER2 positive or metastatic cancer
  • Any other primary tumor
  • Contraindication to moderate physical activity
  • Contraindication to adjuvant chemotherapy or radiotherapy
  • Pregnancy or breast feeding
  • Inability to attend or comply with interventions or follow-up scheduling, disability or difficulty preventing a proper understanding of trial

Treatment and study plan

Tailored program of PA and nutritional counseling

Behavioral

Patients receive tailored program of physical exercises and nutritional counseling during the course of adjuvant treatments (CT followed by RT, 27 weeks).

Primary outcomes

  1. Subjective fatigue

    Time frame: At 18 months

    Subjective fatigue is measured using the Multidimensional Fatigue Inventory (MFI-20) questionnaire

Secondary outcomes

  1. Quality of life

    Time frame: At 18 months

    Quality of life is measured by the EORTC QLC-C30 questionnaire

  2. Anxiety/depressive symptoms

    Time frame: At 18 months

    Anxiety/depressive symptoms is measured by the HADS questionnaire

  3. Physical activity level

    Time frame: At 18 months

    Physical activity level is measured by the GPAQ questionnaire

  4. Muscular fatigue

    Time frame: At 18 months

    Muscular fatigue is measured by Myotest

  5. Attention fatigue

    Time frame: At 18 months

    Attention fatigue is measured usingt the TAP 2.2 software

  6. Body Mass Index

    Time frame: At 18 months

    Body Mass Index is calculated using bodyweight and length measurements

  7. Body composition

    Time frame: At 18 months

    Body composition (fat mass/fat-free mass ratio) is assessed by dual-energy X-ray absorptiometry (DEXA)

Sponsors and collaborators

Lead sponsor

Institut du Cancer de Montpellier - Val d'Aurelle

Other

Registry information

Official study title

A Randomized Controlled Trial to Evaluate the Effect of a Tailored Program of Physical Activity and Nutritional Counseling on Fatigue Reduction in Breast Cancer Patients Receiving Adjuvant Treatment.

Acronym: APAD

Important dates

Study start
2010
Primary completion
2014
Study completion
2014
First posted
Dec 20, 2011
Registry last updated
Aug 21, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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