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iPad Use in Reducing Anxiety and Depression in Patients Undergoing Bone Marrow Transplant

Project BUCKiPAD: The Evaluation of an iPAD Distribution Program on Anxiety and Depression in Bone and Marrow Transplant Patients

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02378012
Acronym
BUCKiPAD
Enrollment
6
Registered
2015-03-04
Start date
2014-03-19
Completion date
2014-09-06
Last updated
2020-06-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anxiety, Depression, Malignant Neoplasm

Brief summary

This randomized clinical trial studies iPad use in reducing anxiety and depression in patients undergoing bone marrow transplant. A tablet device like the iPad can provide access to music, television, movies, books, and the Internet. It also contains a video conferencing system that can allow patients to communicate with family members and other members of their social support team. With these capabilities, an iPad distribution program may help lessen patient anxiety and depression during a hospital stay. Monitoring iPad use by patients may help doctors better understand how patients use their computers and tablets while in the hospital so that the software and applications of the iPad can be made more useful.

Detailed description

PRIMARY OBJECTIVES: I. To evaluate the effect access to an iPad has on anxiety as measured by the Hospital Anxiety and Depression Scale. SECONDARY OBJECTIVES: I. Determine how computers and tablets are used by patients who have access to such devices. OUTLINE: Participants are assigned to Group A or randomized to 1 of 2 groups (Groups B or C). GROUP A (participants provide their own computer or tablet device): A member of the research personnel helps the participants install Netflix, Spotify, and Skype applications on their computers if they wish to do so. Participants will be given subscriptions to each application and usernames for access on days -5 to 10. GROUP B (Apple iPad): Participants receive an iPad for days -5 to 10. Participants also receive the BuckiPad manual for instructions on how to use the iPad and Netflix, Skype, and Spotify applications. Participants are also directed to the official Apple's iPad user's manual on their device and have questions answered by research personnel on day -5. GROUP C: Participants do not receive an iPad for days -5 to 10.

Interventions

Receive access to Netflix, Spotify, and Skype applications

OTHERQuestionnaire Administration

Ancillary studies

Sponsors

Ohio State University Comprehensive Cancer Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adult patients undergoing treatment in the bone marrow transplant (BMT) unit on the 3rd floor of the James Cancer Hospital and Solove Research Institute * Patients receiving reduced intensity chemotherapy for an allogeneic stem cell transplant

Exclusion criteria

* Patients who lack the visual or motor skills necessary to use a tablet device like the Apple iPad * Criteria for visual proficiency will be determined by asking the patient: do you have trouble reading a newspaper even with your glasses or contacts (if you wear them); if yes, they will be excluded * Criteria for motor skill proficiency will be determined by asking the patient: do you have any trouble using a television remote control; if yes, they will be excluded * Patients who do not speak English

Design outcomes

Primary

MeasureTime frameDescription
Change in Hospital Anxiety and Depression Scale (HADS)-Anxiety scoreBaseline to day 10Will be analyzed using an analysis of covariance (ANCOVA) model containing fixed effects of treatment condition (iPAD vs. no iPAD), baseline HADS-Anxiety score, and a random, normally distributed error term. The data will be log-transformed prior to analysis, so all resulting inferences will be based on the geometric mean instead of the arithmetic mean.

Secondary

MeasureTime frameDescription
Change in HADS depression scoreBaseline to day 10Will be analyzed using an ANCOVA model containing fixed effects of treatment condition (iPAD vs. no iPAD), baseline HADS-Depression score, and a random, normally distributed error term. The data will be log-transformed prior to analysis, so all resulting inferences will be based on the geometric mean instead of the arithmetic mean.
Change in Profile of Mood States Short Form (POMS-SF) scoresBaseline to day 10Will be analyzed using an ANCOVA model containing fixed effects of treatment condition (iPAD vs. no iPAD), baseline POMS-SF score, and a random, normally distributed error term. The data will be log-transformed prior to analysis, so all resulting inferences will be based on the geometric mean instead of the arithmetic mean.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026