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Completed

NCT Number: NCT00721383

Telephone Resources and Assistance for Caregivers (TRAC)

The purpose of this randomized clinical trial is to test a 12-month multi-component health promotion intervention with home-based family caregivers of persons with Alzheimer's Disease and other related dementias. Specific aims are to: 1) Test the primary hypothesis: The Enhancing Physical Activity treatment intervention will be more effective in increasing caregiver lifestyle physical activity than the Standard Care Intervention; 2) Test secondary hypotheses: The Enhancing Physical Activity treatment intervention will be more effective than the Standard Care Intervention in improving the following caregiver secondary outcomes: mental health, physical health and physical function; and 3) Evaluate the process of implementing a lifestyle physical activity intervention with family caregivers. The Standard Care Intervention focuses on well-established care-related education and support needs. The Enhancing Physical Activity treatment intervention focuses on two areas: increasing lifestyle physical activity and addressing well-established care-related concerns that are likely to interfere with increasing physical activity. A total of 190 middle-age to older community-based primary caregivers of persons with Alzheimer's disease or other related dementias who report some to moderate strain with caregiving activities will be randomly assigned to either the Enhancing Physical Activity or Standard Care Intervention. Data will be collected at baseline, 3, 6, 9, 12 and 18 months and include self-report and direct observational methods. Data will be analyzed by using repeated measures models using the generalized estimating equation approach. Family caregivers are a stressed population who experience changes in their mental and physical health. However, effect sizes have been minimal for interventions designed to only affect caregiver mental health. No study known to us, has tested the added value of physical activity adoption in conjunction with more traditional caregiver support and skill building. Study findings will enable us to evaluate the behavioral , physical, and health-related quality of life effects achieved by the combined intervention; and will add knowledge about the most effective ways of intervening with family caregivers and other chronically stressed middle-age and older adult populations.

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Key information

Age range

40 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Stanford University School of Medicine, Stanford, California, United States

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Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Care recipient:

  • Diagnosis of probable AD or related dementia (using NINCDS/ADA criteria)
  • Reside in the community
  • Receive assistance from a primary caregiver

Caregiver:

  • Are a spouse or other close family member of the person with AD/dementia
  • Age ≥ 40 years
  • English-speaking
  • Live with the care recipient (or close as in 5-10 miles)
  • Provide ≥ 10 hours of care per week
  • Caregiver for at least 6 months
  • Are physically inactive, defined as accumulating ≤ 60 minutes of regular PA on a weekly basis for the past 6 months
  • Reporting some to moderate levels of strain
  • Are cognitively intact
  • Have no major debilitating health problems that would prevent intervention participation
  • Must have a telephone
  • Willing to increase levels of physical activity
  • Agree to assignment of treatment condition

Exclusion criteria

Care receiver:

  • Other dementias such as stroke or Parkinson's
  • Terminal illness with life expectancy of less than six months
  • Bedfast or confined to a bed or chair at least 22 hours a day for at least 3 of the previous 7 days
  • ≥ 3 acute or medical or psychiatric hospitalizations in last year

Caregiver:

  • Are involved in another caregiver clinical trial
  • Have a terminal illness with life expectancy of less than 6 months
  • Receiving active treatment for cancer

Treatment and study plan

Enhancing Physical Activity Intervention

Behavioral

Physical activity and caregiver skill-building

Other names: EPAI

CSBI

Behavioral

Caregiver skill-building

Primary outcomes

  1. self-reported physical activity

    Time frame: 18 months

Secondary outcomes

  1. caregiving burden

    Time frame: 18 months

  2. caregiver positive well-being

    Time frame: 18 months

  3. self-reported physical health

    Time frame: 18 months

  4. physical function

    Time frame: 18 months

Sponsors and collaborators

Lead sponsor

Rush University Medical Center

Other

Collaborators

  • Stanford University

Registry information

Official study title

Clinical Trial to Enhance Caregiver Physical Activity

Acronym: TRAC

Important dates

Study start
2007
Primary completion
2013
Study completion
2013
First posted
Jul 24, 2008
Registry last updated
Dec 31, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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