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Spots Global Cancer Trial Database for A Feasibility Study of the Use of Actigraphy to Determine Prognosis in Patients With Advanced Cancer

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Trial Identification

Brief Title: A Feasibility Study of the Use of Actigraphy to Determine Prognosis in Patients With Advanced Cancer

Official Title: A Feasibility Study of the Use of Actigraphy to Determine Prognosis in Patients With Advanced Cancer

Study ID: NCT03283683

Conditions

Cancer
Sleep

Interventions

Study Description

Brief Summary: This study evaluates the use of actigraphy-derived measures to improve prognostication in patients with advanced cancer.

Detailed Description: An accurate assessment of prognosis (life expectancy) is important for cancer patients, their carers, and their health care professionals. In the case of patients / their carers, it allows them to plan for the future, and to make more informed decisions about further anti-cancer treatments, and about referral to supportive and palliative care services. However, previous research suggests that health care professionals are not particularly good at estimating prognosis, and frequently over-estimate prognosis. The aim of this project is to assess the usefulness of measuring physical activity, and differences between daytime and nighttime physical activity, in determining prognosis in patients with cancer. Studies suggest that these measures may be useful in determining prognosis in certain groups of patients with cancer (e.g. patients receiving chemotherapy for colon / rectum cancer). However, these studies need to be repeated in patients with different types of cancer, and also patients receiving other types of treatment (including supportive and palliative care). The aim of this small scale ("feasibility") study is to determine whether or not a large scale ("definitive") study can be done. The feasibility study will include 50 patients with cancer, who will be asked to rate their performance status (physical activity) on a well-used scale, and then to wear a watch-like device for one week that measures physical activity and sleep patterns. The researcher will collect a blood sample: some of which will be used for analysis of parameters, which have previously been identified as prognostic indicators and will collect and store some blood for future transcriptome analysis. Participants will also be asked to complete a sleep diary during the week, and a questionnaire about their symptoms at the beginning and end of the week. The study will last one week in total and is collaboration between the Royal Surrey County Hospital, and the University of Surrey (Surrey Sleep Research Centre).

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Royal Surrey County Hospital, Guildford, Surrey, United Kingdom

Contact Details

Name: Derk-Jan Dijk

Affiliation: Supervisor

Role: STUDY_DIRECTOR

Name: Andrew Davies

Affiliation: Supervisor

Role: STUDY_DIRECTOR

Name: Shuchita D Patel

Affiliation: PhD student

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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