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The Cancer Home Life Intervention Study. A Randomised, Controlled Multicentre Trial and a Health Economic Evaluation

The Cancer Home Life Intervention Study Protocol: Effectiveness on Everyday Activities and Quality of Life in People With Advanced Cancer Living at Home. A Randomised, Controlled Multicentre Trial and a Health Economic Evaluation

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02356627
Enrollment
242
Registered
2015-02-05
Start date
2015-02-01
Completion date
2017-03-31
Last updated
2017-05-10

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

Conditions

Activities of Daily Living, Cancer, Everyday Activities, Palliative Care, Quality of Life

Keywords

Occupational therapy, Adaptive intervention, Home-based, Assistive Technology, Home modification, Clinical effectiveness, Cost-effectiveness, Cost-utility

Brief summary

The purpose of this study is to examine the effectiveness and cost-effectiveness of the Cancer Home Life Intervention compared to usual care on performance of and participation in everyday activities and quality of life in people with advanced cancer living at home.

Detailed description

The sample size is based on the primary outcome measure: the mean Activty of Daily Living (ADL) motor ability 1.04 logits (SD 0.727) as measured by the Assessment of Motor and Process Skills (AMPS). A significance level of 0.05 would provide 80% power to detect a between-group difference of 0.3 logits requiring a sample size of N=184. An expected drop-out rate of 32% at 3 months follow-up means that 272 patients with advanced cancer must be included in the study from three hospitals. Multiple imputation will be used to estimate a plausible value for missing data of participants that are lost to follow-up due to other reasons than death. This does not, however, apply to the primary outcome data where no estimations will be computed. For normally distributed ratio data the intervention group will be compared with the control group using multiple linear regression analysis of mean changes from baseline. Logistic regression analysis will be used for ordinal data. Adjustments for hospital and for baseline values will be made. A modified intention-to-treat analysis will be applied. Subgroup analyses to identifiy groups that especially benefit from the intervetnion will be performed. The cost-effectiveness analysis wil be performed with ADL motor ability as the clinical parameter, and the cost-utility analysis will be based on the calculation of Quality Adjusted Life Years (QALY). The Incremental Cost-effectiveness Ratio (ICER) will be calculated and the results summarised in a cost-effectiveness acceptability curve (CEAC).

Interventions

OTHERThe Cancer Home Life Intervention

Adaptive interventions aiming at compensating for functional limitations.

Sponsors

University of Southern Denmark
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

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

Inclusion criteria

* ≥18 years old * Diagnosed with cancer * Evaluated incurable by responsible oncologist in respective out-patient unit * Functional level 1-2 on the WHO performance scale * Live within a radius of maximum 60 km from AUH or NH or on the island of Funen * Live in a private home or in sheltered living * Know sufficient Danish to fill out questionnaires and participate in interviews.

Exclusion criteria

* Cognitive impairment preventing the participants from participating in a structured interview * Live in a nursing home or a hospice * Considered incapable of complying with the trial

Design outcomes

Primary

MeasureTime frameDescription
Activity of Daily Living (ADL) motor ability as measured by the Assessment of Motor and Process Skills (AMPS)3 monthsObserved quality of Activity of Daily Living (ADL) motor ability

Secondary

MeasureTime frameDescription
Individually Prioritised Problems Assessment (IPPA)6 weeks and 3 monthsEveryday activities that the participant has problems with and prioritise to have solved
Everyday activity pattern captured by a One Day Diary3 monthsThe participant records every ½ hour what he/she does, where, is together with, how he/she feels mentally and physically
Impact on Participation and Autonomy Questionnaire (IPAQ)6 weeks and 3 monthsAutonomy and participation is assessed regarding autonomy indoors, family roles, and social life and relationships
The European Organization for Research Treatment of Cancer Quality of Life Questionnaire Core 30 (EORTC QLQ C-30)6 weeks and 3 monthsCancer specific health-related quality of life
EuroQol 5-dimensions 5 levels (EQ-5D-5L)6 weeks, 3 months, and 6 monthsHealth-related quality of life

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 7, 2026