Animal Assisted Activity Program on Patients and Staff on an Inpatient Surgical Oncology Unit

Sponsor
Memorial Sloan Kettering Cancer Center (Other)
Overall Status
Completed
CT.gov ID
NCT02363608
Collaborator
(none)
146
1

Study Details

Study Description

Brief Summary

The purpose of this study is to describe the effects of canine-assisted activity visits on patients and staff in a hospital setting. The Caring Canines program uses dogs who have been trained to be obedient, calm and comforting. It involves a visit by a volunteer (called the dog's handler) and the volunteer's dog that has been trained and tested to have a good personality and to follow commands. A visit typically lasts about 10-15 minutes with the patient interacting with the dog while the dog is supervised by the handler. Memorial Sloan Kettering currently has Caring Canine dogs visit patients but the investigators don't yet know the impact of these visits on patients and staff. The investigators would like to see how the Caring Canine visits impact a patients' mood, including anxiety, stress, and sense of well-being. Two groups of patients will take part in this study - the first group will receive standard post surgery care and will not receive a visit from the Caring Canines program and the second group will receive daily visits (Tuesday -Friday) from the Caring Canines program while they are on M15. The purpose of this study is to look at differences in well-being between patients who have the visits with the dogs and patients who do not.

Condition or Disease Intervention/Treatment Phase
  • Other: standard post surgery care
  • Behavioral: Caring Canine program
  • Behavioral: baseline and post assessment

Study Design

Study Type:
Observational
Actual Enrollment :
146 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Caring Canines: Outcomes From an Animal Assisted Activity Program on Patients and Staff on an Inpatient Surgical Oncology Unit
Study Start Date :
Jan 1, 2015
Actual Primary Completion Date :
Jan 1, 2017

Arms and Interventions

Arm Intervention/Treatment
standard post surgery care

An initial cohort of consecutive patients admitted to the 15th floor of the hospital on a Monday or Tuesday will form the usual care control arm of the study. Once this cohort is completed, the Caring Canines program will start.

Other: standard post surgery care

Caring Canines program

Once the standard of care cohort is completed, the Caring Canines program will start making visits on the 15th floor and a second cohort of consecutive patients admitted to M15 on a Monday or Tuesday will form the intervention (experimental) arm of the study.patients admitted to M15 on a Monday or Tuesday will form the intervention (experimental) arm of the study.

Behavioral: Caring Canine program
The therapy dogs who visit at MSKCC. A visit by a therapy dog typically lasts about 10-15 minutes with the patient interacting with the therapy dog while the dog is supervised by the handler.

Behavioral: baseline and post assessment
The baseline and post assessment will include the Professional Quality of Life Scale (ProQOL R-IV) (Stamm, 1997-2005) and qualitative questions.

staff canine-assisted

For the staff portion of this study a longitudinal pre and post intervention design will be used. Baseline staff assessments will occur prior to the Caring Canine program being implemented on the unit. The assessments include questions about compassion satisfaction and compassion fatigue as well as some open ended questions about your thoughts on the Caring Canines program. Post assessment will occur after the program has been active on the unit for at least 6 weeks. Only staff who work at least one Monday - Friday day shift each week will be eligible to participate.

Behavioral: Caring Canine program
The therapy dogs who visit at MSKCC. A visit by a therapy dog typically lasts about 10-15 minutes with the patient interacting with the therapy dog while the dog is supervised by the handler.

Behavioral: baseline and post assessment
The baseline and post assessment will include the Professional Quality of Life Scale (ProQOL R-IV) (Stamm, 1997-2005) and qualitative questions.

Outcome Measures

Primary Outcome Measures

  1. change from baseline in the follow-up PHQ-4 scores [1 year]

    The PHQ-4 is an ultra-brief self-report questionnaire that consists of a 2-item depression scale and a 2 item anxiety scale. Among the control and intervention groups to assess psychological effects of the program. Responses on the pain scale will assess physiological effects, and responses on the open-ended questions will identify patient-perceived benefits of the program

  2. difference in baseline and follow-up ProQOL scores (For Staff) [1 year]

    (Compassion Satisfaction score and Burnout score) to assess change in work satisfaction due to the program, and responses on the qualitative questions will address staff-perceived benefits of the program.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:

Patients

  • Age greater than 21

  • Admitted to M15 following a Monday or Tuesday surgery

  • Ability to speak and read English.

Staff

  • Age greater than 21

  • Works at least one day shift a week on M15

  • Ability to speak and read English

Exclusion Criteria:

Patients

  • Self reported allergy to dogs

  • Medical need to be in an isolation room

  • Medical need to be in a Protective Environment room .

Staff

  • Self reported allergy to dogs

Contacts and Locations

Locations

Site City State Country Postal Code
1 Memorial Sloan Kettering Cancer Center New York New York United States 10065

Sponsors and Collaborators

  • Memorial Sloan Kettering Cancer Center

Investigators

  • Principal Investigator: Pamela Ginex, EdD, RN, OCN, Memorial Sloan Kettering Cancer Center

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

None provided.
Responsible Party:
Memorial Sloan Kettering Cancer Center
ClinicalTrials.gov Identifier:
NCT02363608
Other Study ID Numbers:
  • 15-010
First Posted:
Feb 16, 2015
Last Update Posted:
Jan 13, 2017
Last Verified:
Jan 1, 2017
Keywords provided by Memorial Sloan Kettering Cancer Center

Study Results

No Results Posted as of Jan 13, 2017