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Positive Psychology Intervention to Improve Quality of Life in Stem Cell Transplant Survivors and Their Caregivers

Fred Hutchinson Cancer Center (FHCC) logo

Fred Hutchinson Cancer Center (FHCC)

Status

Completed

Conditions

Hematopoietic Cell Transplantation Recipient

Treatments

Other: Quality-of-Life Assessment
Behavioral: Telephone-Based Intervention
Behavioral: Booklet
Other: Survey Administration
Behavioral: Exercise Intervention

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT03525106
9969 (Other Identifier)
P30CA015704 (U.S. NIH Grant/Contract)
NCI-2018-00541 (Registry Identifier)

Details and patient eligibility

About

This trial studies a positive psychology intervention designed to improve quality of life in stem cell transplant survivors and their caregivers. Positive psychology (PP) uses systematic exercises (e.g., gratitude letters, acts of kindness) to potentially boost levels of optimism, resilience, and life enjoyment. PP interventions are often enjoyable, easy to understand, and can be delivered via telephone. PP intervention may improve the quality of life of participants who have undergone a stem cell transplant or their caregivers.

Full description

PRIMARY OBJECTIVES:

I. Pilot a positive psychology intervention delivered to hematopoietic cell transplantation (HCT) survivors and interested caregivers over an 8 week period.

II. Determine the proportion of patients who enroll and the immediate benefit to participants, as measured by pre- and post-exercise measures of happiness and optimism.

III. Pilot outcome data collection mechanisms in preparation for a randomized clinical trial.

OUTLINE:

Participants and caregivers receive a positive psychology exercise manual, complete positive psychology exercises every week, and participate in phone sessions over 30 minutes every week for 8 weeks.

After completion of study, participants are followed up at 6 months.

Enrollment

29 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Written informed consent
  • English as primary language
  • At least 1 year after HCT

Exclusion criteria

  • Major psychiatric diagnosis that impairs cognitive functioning or is not controlled at the time of the approach.
  • Medical conditions precluding participation in the intervention or likely to lead to death within 6 months, as determined by the principal investigator (PI)

Trial design

Primary purpose

Supportive Care

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

29 participants in 2 patient groups

Participants: Positive Psychology Intervention
Experimental group
Description:
Participants receive a positive psychology exercise manual, complete positive psychology exercises every week, and participate in phone sessions over 30 minutes every week for 8 weeks.
Treatment:
Other: Survey Administration
Behavioral: Telephone-Based Intervention
Behavioral: Booklet
Behavioral: Exercise Intervention
Other: Quality-of-Life Assessment
Caregivers: Positive Psychology Intervention
Experimental group
Description:
Caregivers receive a positive psychology exercise manual, complete positive psychology exercises every week, and participate in phone sessions over 30 minutes every week for 8 weeks.
Treatment:
Other: Survey Administration
Behavioral: Telephone-Based Intervention
Behavioral: Booklet
Behavioral: Exercise Intervention
Other: Quality-of-Life Assessment

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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