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HomeboundNCT00248924

Outcomes Of Social Service Programs For Homebound Older Adults

An observational study of Homebound and Elderly, run by Weill Medical College of Cornell University at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The objective of this prospective study is to document the impact of social service interventions (including meals, telephone reassurance, and friendly visiting)provided by the Burden Center, a model community social service agency, on overall quality of life. Read more about this study

Who is it for?
Ages 60 years and older
Conditions the study is for
Homebound, Elderly
What is being tested?
Social Services
How many people
56 participants
Where
1 siteUnited States
Study dates
Apr 2001to Feb 2003
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 60 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • All new clients of the Burden Center for the Aging who are homebound, out of the home less than one time per week, and cognitively intact will be eligible for enrollment.

Who cannot join

  • Clients unable to give informed consent such as those suffering from a major psychiatric disease or those who are not cognitively able to give informed consent will be excluded.
  • Clients who refuse to participate will be excluded

Trial locations and contacts

1 site in 1 country.

United States1 site
  • The New York Presbyterian Hospital-Weill Medical Center

    New York, New York, 10021

Other trials in United States

About this study

The objective of this prospective study is to document the impact of social service interventions (including meals, telephone reassurance, and friendly visiting)provided by the Burden Center, a model community social service agency, on overall quality of life.

Read the detailed description

Specific outcomes include mental and physical function as measured by the SF-36, and depressive symptoms as measured by the CES-D depression scale. The hypothesis is that a multicomponent social service intervention program that provides social support and reduces social isolation can prevent depression and decline in quality of life in this vulnerable population.

Conditions
Homebound, Elderly
Being tested
Social Services
Keywords
Social service intervention, Social support, Elderly, Homebound, Quality of life

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Social ServicesBehavioural

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Quality of life Depressive symptoms

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted4 Nov 2005 (estimated)
  2. Study startApr 2001
  3. Study completionFeb 2003

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Time perspective
Prospective
Enrolment
56 participants
IDs, dates and publications
ClinicalTrials.gov ID
NCT00248924
Sponsor's protocol ID
0101-561
Status last verified
Mar 2008
First submitted
13 Sep 2005
Last updated
3 Apr 2008
Results posted
No
Data monitoring committee
No

Publications

  • Charlson ME, Peterson JC, Syat BL, Briggs WM, Kline R, Dodd M, Murad V, Dionne W. Outcomes of community-based social service interventions in homebound elders. Int J Geriatr Psychiatry. 2008 Apr;23(4):427-32. doi: 10.1002/gps.1898.

    PubMed 17918183

Questions about this trial

What is this clinical trial studying?

An observational study of Homebound and Elderly, run by Weill Medical College of Cornell University at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 3 Apr 2008. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Quality of life Depressive symptoms. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT00248924, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 3 Apr 2008.

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