PEACH Trial: Prescribed Exercise After Chemotherapy (PEACH)
Individually Prescribed Exercise Versus Usual Care in a Heterogeneous Cancer Survivor Population: A Pragmatic Randomized Controlled Trial
Many cancer survivors suffer symptoms such as fatigue and dyspnea which may persist for years or months after their chemotherapy has finished. Despite the known benefits of exercise and its potential to address many of the symptoms after cancer, the type of practical exercise programme which best suits this population is not known.
Many exercise programmes performed in cancer survivors take place over many weeks or months and include people with specific types of cancer. Such programmes may therefore not be suitable for the majority of cancer survivors and would pose serious practical difficulties with high drop-out rates and expensive resource consumption if they were extended into clinical practice.
We propose to run an 8-week exercise intervention in a mixed cancer population.
Hypothesis: A brief, individually tailored 8-week intervention will increase fitness and improve other physical symptoms in a mixed cancer survivor population after chemotherapy.
Studieoversikt
Detaljert beskrivelse
Background: Many cancer survivors suffer a range of physical and psychological symptoms with may persist for years or months after treatment finishes. Despite the known benefits of exercise and its potential to address many of these adverse effects of treatment, the role of exercise as well as its optimum duration, frequency, and intensity in this population has yet to be fully elucidated. Many cancer rehabilitation programmes presented in the literature are very long, have tight eligibility criteria and are not likely to be practical in the majority of cancer survivors. We plan to investigate a novel brief 8-week intervention which aims to increase physical fitness, and address other physical symptoms in a heterogeneous cancer survivor population.
Methods/design: Approximately 60 cancer survivors 2-6 months after completion of chemotherapy, usually adjuvant, with curative intent will be recruited through oncology clinics in a single institution and randomised to usual care or an exercise intervention. The exercise intervention consists of two specifically tailored, supervised, moderate intensity aerobic exercise sessions per week for 8 weeks. All participants will be assessed at baseline (0 weeks), post intervention (8 weeks), and at 3-month follow-up. The primary outcome measure is fitness, and secondary patient-related outcome measures include fatigue, quality of life, and morphological outcomes. A further secondary outcome is process evaluation including adherence to and compliance with the exercise program.
Discussion: This study will provide valuable information about the physical outcomes of this 8-week supervised aerobic programme. Additional process information and economic evaluation will inform the feasibility of implementing this program in a heterogeneous population after chemotherapy treatment with curative intent.
Studietype
Registrering (Faktiske)
Fase
- Fase 3
Kontakter og plasseringer
Studiesteder
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Dublin, Irland, 8
- Medical Oncology Department, St. James's Hospital
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Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Beskrivelse
Inclusion Criteria:
- Diagnosis of solid tumour and completion of adjuvant chemotherapy (and/or radiotherapy) with curative intent within the preceding 2-6 months. (Patients who have received neoadjuvant chemotherapy or chemoradiotherapy followed by surgery will also be eligible. In addition, patients continuing onto adjuvant hormone therapy and anti-Her2 directed therapy are eligible).
- Ability to understand English
- Willing to be randomised
- Medical clearance to exercise
- Age 21-69
- Fitness level average, fair or poor according to certain pre-determined cut-off points for age and gender(Fletcher et al., 2001)
- Willing and able to attend supervised exercise sessions twice weekly for a period of 8 weeks, with an intention of achieving > 90% attendance
- LVEF > 50% and not < 20% worse than baseline in applicable patients
Exclusion Criteria:
- Evidence of active cancer
- Chronic medical and orthopaedic conditions that would preclude exercise (eg uncontrolled congestive heart failure or angina, recent MI, breathing difficulties requiring oxygen use or hospitalization)
- On beta-blocker medication
- Prior history of another cancer in previous 5 years (exception: non-melanoma skin cancer and non-invasive cancer of the cervix)
- Confirmed pregnancy
- Dementia or psychiatric illness that would preclude ability to participate in study
- Incomplete haematological recovery after chemotherapy (WCC< 3, Hb < 10 or Platelets < 100)
- BMI > 35
- LVEF post chemotherapy < 50% or > 20% deterioration of baseline pre-systemic treatment. LVEF criteria are applicable in patients who have received chemotherapy deemed in normal clinical practice to have a potential effect LVEF and in whom the LVEF will have been measured before systemic treatment and at end of chemotherapy
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Enkelt
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
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Aktiv komparator: Exercise Programme
This will consist of an 8-week exercise programme, performed twice per week.
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Moderate intensity exercise
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Placebo komparator: Usual Care
Standard practice including opportunistic exercise advice and patients' self-directed physical activity
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Moderate intensity exercise
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Hva måler studien?
Primære resultatmål
Resultatmål |
Tidsramme |
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Modified Bruce Treadmill Test (Fitness)
Tidsramme: 0, 8 weeks, 3 months
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0, 8 weeks, 3 months
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Sekundære resultatmål
Resultatmål |
Tidsramme |
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FACT-G scale (Quality of life-overall)
Tidsramme: 0, 8 weeks, 3 months
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0, 8 weeks, 3 months
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FACT-F (Fatigue)
Tidsramme: 0, 8 weeks, 3 months
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0, 8 weeks, 3 months
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RT3 Accelerometry (Activity level)
Tidsramme: 0, 8 weeks, 3 months
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0, 8 weeks, 3 months
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Tanita Body Fat Assessment (% fat)
Tidsramme: 0, 8 weeks, 3 months
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0, 8 weeks, 3 months
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SF-36v2 (Quality of life-functional aspects)
Tidsramme: 0, 8 weeks and 3 months
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0, 8 weeks and 3 months
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Samarbeidspartnere og etterforskere
Samarbeidspartnere
Etterforskere
- Hovedetterforsker: Dearbhaile O' Donnell, MD, St. James's Hospital, Dublin, Ireland
- Hovedetterforsker: Juliette Hussey, PhD, Trinity College Dublin, Ireland
- Hovedetterforsker: Julie M Walsh, MSc, University of Dublin, Trinity College
Publikasjoner og nyttige lenker
Studierekorddatoer
Studer hoveddatoer
Studiestart
Primær fullføring (Faktiske)
Studiet fullført (Faktiske)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Anslag)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Anslag)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Andre studie-ID-numre
- CTPF/2008/12
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