An Evaluation of the Determinants of Lifestyle and Health Behaviors in Later Life
NCT ID: NCT02574416
Last Updated: 2018-12-06
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
86 participants
OBSERVATIONAL
2015-02-28
2018-12-31
Brief Summary
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Detailed Description
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Patients who have used the same Medicine for Older People Services in Southampton within the previous year will be known to the medical team. The medical team will write to the patient with a letter of invitation to participate in the study and the Patient Information Sheet. The letter will contain a reply slip and a stamped addressed envelope. It will also contain contact details should the patient wish to talk to someone about the study and what it would mean for them to participate. Patients who send back their reply slip saying that they would like to participate in the study will be contacted to arrange a home visit at a convenient time. If no reply slip is received after two weeks then a member of the research team will telephone the patient once to find out whether they have received the letter and to offer them the opportunity to participate. This will be done sensitively and carefully and the patients' wishes will be respected at all times. Written informed consent will be taken at the time of the home visit.
All participants will be visited at home by a member of the research team who will interview the participant to obtain background sociodemographic information and a series of short questionnaires will be administered. Each participant will have an assessment of diet quality, appetite and physical function. In addition, weight, grip strength and physical performance will be measured. Participants will be free to decline any part of the questionnaire or assessment.
Two and a half years after this interview the investigators will check on the hospital administration system if the participant's contact details have changed or if they have died since the initial visit. The investigators will then contact the participant by phone (having gained permission to do this at the original assessment visit) to arrange a home visit when diet quality, appetite and physical function will be reassessed. The investigators' experience from the Southampton Mealtime Assistance Study of contacting older study participants by telephone has shown this to be an effective way of ascertaining if the participant is interested in continuing with the study or would prefer not to. The participant will be given the opportunity to refuse a visit with no pressure applied. At the visit the investigators will also ask about the participants' use of the key community services over the past year. The investigators will also ask permission to access the patient's medical records to obtain details of hospital admissions or outpatient appointments in the intervening year.
Conditions
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Study Design
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CASE_ONLY
OTHER
Interventions
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There is no intervention
The study is observational and there is no intervention
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* acutely unwell
60 Years
110 Years
ALL
No
Sponsors
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National Health Service, United Kingdom
OTHER_GOV
Responsible Party
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Sian Robinson
Professor of Nutritional Epidemiology
Principal Investigators
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Sian Robinson, PhD
Role: PRINCIPAL_INVESTIGATOR
National Health Service, United Kingdom
Locations
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MRC Lifecourse Epidemiology Unit
Southampton, Hampshire, United Kingdom
Countries
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Other Identifiers
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RHM MED 1215
Identifier Type: -
Identifier Source: org_study_id
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