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Program of Exercise, Diet and Control of Psychological Stress in Cancer Survivors

Evaluation of the Effects of Exercise, Diet and Control of Psychological Stress in Cancer Survivors

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01108484
Acronym
EDICOS
Enrollment
140
Registered
2010-04-22
Start date
2010-03-31
Completion date
2015-08-31
Last updated
2020-11-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cancer Survivors

Keywords

Cancer survivors, exercise, diet, emotional support

Brief summary

A program of exercise, diet and psycho-emotional support could improve some outcomes in cancer survivors.

Detailed description

Cancer survivors will be randomised to one of the following groups: a) Supervised physical activity, b) Supervised physical activity + Diet counseling, c) Supervised physical activity + Diet counseling + psycho-emotional support

Interventions

BEHAVIORALExercise

Supervised exercise: Three 90-minutes sessions per week.

BEHAVIORALExercise + Diet counseling

Supervised exercise: Three 90-minutes sessions per week. Diet counseling: Counseling to balance the intake.

BEHAVIORALExercise + Diet counseling + psycho-emotional support

Supervised exercise: Three 90-minutes sessions per week. Diet counseling: Counseling to balance the intake. Psycho-emotional support: Weekly sessions to modify the behaviour.

Sponsors

Grupo de Investigación en Actividad Física y Salud
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* cancer survivors attending their follow-up visits

Exclusion criteria

* Cardiac disease NYHA II * non-controlled hypertension * non-controlled metabolic disease * chronic infectious disease * non-controlled pain * risk of bone fracture * severe anemia, leucopenia or thrombopenia

Design outcomes

Primary

MeasureTime frameDescription
VO2 maxbasal, 6, 12 and 24 monthsthe highest rate of oxygen consumption attainable during maximal exercise

Secondary

MeasureTime frameDescription
Physical Activity Quality of life Food intake Anxiety and Psychological Distressbasal, 6, 12 and 24 monthsMeasured through accelerometer, PAR, CFCA, EORTC QLQ C-30 and SF-36

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026