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Life Enhancing Activities for Family Caregivers (LEAF)

University of California San Francisco (UCSF) logo

University of California San Francisco (UCSF)

Status

Completed

Conditions

Affect
Dementia
Stress

Treatments

Behavioral: Positive Affect

Study type

Interventional

Funder types

Other

Identifiers

NCT01825681
14-13236
A115168 (Other Grant/Funding Number)

Details and patient eligibility

About

Life Enhancing Activities for Family Caregivers is a six-week program designed to increase positive affect in people who care for a family member with dementia. The intervention consists of 6 weekly one-hour sessions conducted one-on-one with a trained facilitator to teach simple skills that are practiced at home in a study-supplied workbook. The program is preceded and followed by a 30-45 minute questionnaire. Follow-up assessments will be conducted at 1-month, 3-months, and 6-months post intervention.

Primary hypothesis is that experimental subjects who participate in LEAF will demonstrate significantly greater improvements in psychological outcomes and will engage in more problem focused and positive appraisal forms of coping compared to the wait-list control condition.

Full description

All study activities can be conducted from the participant's home, making participation possible for any qualified caregiver with computer and wifi access, in any U.S. state. The LEAF study will supply the tablet computer, software, and workbook required for participation.

Enrollment

175 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Participants must be able to be defined as the primary care provider for a family member with dementia. (Person with dementia must live with the caregiver or in their own home and not in a care facility.)
  • Must speak and read English
  • Must have the ability to provide informed consent

Exclusion criteria

  • Lack of access to a high speed internet connection
  • Evidence of severe cognitive impairment or active psychosis, as assessed by trained interviewers

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Single Blind

175 participants in 2 patient groups

positive affect intervention
Experimental group
Description:
positive affect intervention
Treatment:
Behavioral: Positive Affect
wait list control
No Intervention group
Description:
wait list control

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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