Impact of Hypertrophy-oriented Resistance Training on Muscle Mass and Quality of Life in Patients With Unresectable Pancreatic Cancer

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversidad Europea de Madrid

About this trial

To determine the efficacy of a 12-week supervised, hypertrophy-oriented strength training program in preserving skeletal muscle mass, physical function, and quality of life in patients with unresectable pancreatic cancer compared to standard care.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Diagnosis of locally advanced or metastatic unresectable pancreatic cancer

Undergoing chemotherapy or immunotherapy treatment

Age ≥ 18 years

ECOG score ≤ 2

Disqualifiers

Any relative or absolute contraindication that prevents the performance of training or physical tests.

Diagnosis of other types of primary cancer

Inability to understand Spanish for proper comprehension of the informed consent and questionnaires

Trial design

Design model

Parallel

Treatments tested in this trial

  • supervised, hypertrophy-oriented strength training program

    Other intervention

    12-week supervised, hypertrophy-oriented strength training program in preserving skeletal muscle mass

Treatment groups

10 Participants
are divided into 2 treatment groups
Group A: Intervention GroupExperimental treatment 1 intervention
Group B: Control GroupNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Body Composition

The main objective of this study is to evaluate the effect on body composition (primarily lean mass) through 12 weeks of hypertrophy training in patients with advanced, non-operable pancreatic cancer undergoing treatment

Time frame
Through study completion, an average of 1 year

Secondary outcomes

1

VO2peak

• To analyze whether 12 weeks of hypertrophy training in patients with advanced, unresectable pancreatic cancer receiving chemotherapy and/or immunotherapy has an impact on cardiorespiratory capacity.

Time frame
Through study completion, an average of 1 year
2

Patient-reported outcome measures

• To identify whether 12 weeks of hypertrophy training in patients with advanced, unresectable pancreatic cancer receiving chemotherapy and/or immunotherapy impacts on quality of life. To assess quality of life, the European Organisation for Research and Treatment of Cancer quality of life Questionnaire C30 (EORTC QLQ-C30), version 3.0 will be used. The questionnaire consists of 30 questions grouped into several scales, with higher scores (0-100) indicating better functioning or higher symptom burden.

Time frame
Through study completion, an average of 1 year
3

Anxiety and Depression

• To determine whether 12 weeks of hypertrophy training in patients with advanced, unresectable pancreatic cancer receiving chemotherapy and/or immunotherapy has an impact on anxiety and depression. It will be assesed through the validated questionnaire for assessing anxiety and depression in cancer patients, the Hospital Anxiety and Depression Scale (HADS). It is a 14-item, self-report screening tool used to identify and monitor emotional distress (anxiety and depression) in patients with physical health conditions. It consists of two subscales (7 questions each for anxiety and depression) and is commonly used in hospital settings.

Time frame
Through study completion, an average of 1 year

Other outcomes

Sponsors and contacts

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