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A Clinical Controlled Trial on the Effect of Physical Activity After Cancer Treatment (PACT)

Physical Activity After Cancer Treatment (PACT)- A Clinical Controlled Trial on the Effect of a One-year Physical Activity Program for Cancer Patients Following Cytostatic Treatment

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00717717
Acronym
PACT
Enrollment
214
Registered
2008-07-17
Start date
2006-11-30
Completion date
2012-02-29
Last updated
2015-10-28

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

Conditions

Cancer

Keywords

Cancer Survivor, Physical Activity, Health Behavior, Psychosocial Well-being, Coaching, Long Term, Consequences, Chemotherapy, Motivation

Brief summary

The PACT Study (Physical Activity after Cancer Treatment) is a unique study within the field of cancer rehabilitation in Denmark. It differs from other studies mainly due to the intervention itself. A combination of physiological, health educational and therapeutic elements will be tested. These components are incorporated into a one-year training program for mixed groups (i.e. men + women, with varying cancer diagnoses) to encourage them to enhance their well.-being and quality of life. The overall aim of this approach is to place increased focus on the treated cancer patient's introduction to and exploitation of both physiological and psychosocial yields through physical exercise. Whether or not the study results bear a positive effect, they are expected to support new knowledge in rehabilitation for cancer survivors.

Detailed description

The PACT ('Physical Activity after Cancer Treatment') Study is a multidisciplinary collaborative study carried out by the University Hospitals Centre for Nursing and Care Research (UCSF) and the Finsen Center (Oncology and Hematology Clinics) of the Copenhagen University Hospital (Rigshospitalet), Copenhagen, Denmark. The project draws in cancer patients who have undergone chemotherapy and who are now disease-free or at a stable phase in their illness and have good prognoses. The aim of the study is to investigate the effect of a 12-month rehabilitation program comprising supervised and structured physical exercise training (body conditioning; strength-building; relaxation; massage), patient education and coaching combined with a home-based physical exercise group component and will include a control group. Groups of 12-15 patients will be formed (mixed genders; different oncological and hematological diagnoses) who will train together once weekly during the intervention period. Participation in a training program with peers is seen as a positive motivational factor that stimulates and challenges the patient through physical activity, to use his/her own resources to establish sustainable coping strategies.

Interventions

BEHAVIORALIntervention

One-year rehabilitation program including weekly supervised and group-based physical exercise, home-based physical activity, individual and group-based coaching (narrative therapy), and expert educational talks/lectures

Sponsors

Velux Fonden
CollaboratorOTHER
Danish Cancer Society
CollaboratorOTHER
Rigshospitalet, Denmark
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Cancer diagnosis * Completed cytostatic treatment \<6 months * Affiliated with either the Oncology or Hematology Clinic at the Copenhagen University Hospital, Copenhagen * Between the ages of 15-70 years * No evidence of disease or life expectancy \>2 years.

Exclusion criteria

* Contraindications for physical activity * Bone and brain metastases * Multiple myeloma (in the case of hematological patients) * Symptomatic cardiac illness, including clinical congestive heart disease, treatment caused arrhythmia or myocardial infarction experienced within the previous three months * Dementia and/or psychosis * Patients who cannot read or write Danish.

Design outcomes

Primary

MeasureTime frame
Physical fitness (VO2Max)Baseline and follow-up (6, 12, 18, 24, and 36 months)

Secondary

MeasureTime frame
Muscle strength (1RM) Cholesterol Quality of Life (cancer specific and health related) Anxiety & Depression Fatigue Coping Physical Activity behavior Health BehaviorBaseline and follow-up (6,12,18,24, and 36 months)

Outcome results

None listed

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