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Promoting the Psychological Health of Women With SCI: A Virtual World Intervention

Promoting the Psychological Health of Women With SCI: A Virtual World Intervention

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03543111
Acronym
Zest
Enrollment
175
Registered
2018-06-01
Start date
2018-08-01
Completion date
2021-05-15
Last updated
2022-05-06

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

Conditions

Spinal Cord Injuries

Brief summary

The purpose of this project is to test the efficacy of an internet-based psychological health enhancement program for women with spinal cord injury. The intervention will occur in Second Life (SL), which is an online virtual word simulator with a group of women with spinal cord injury.

Interventions

BEHAVIORALZest

Zest is an internet-based psychological health enhancement program for women with spinal cord injury. The intervention will occur in Second Life (SL), which is an online virtual word simulator with a group of women with spinal cord injury.The Zest program will consist of 10 weekly 2-hour group sessions with approximately 8 women using avatars to represent themselves.

Sponsors

National Institute on Disability, Independent Living, and Rehabilitation Research
CollaboratorFED
TIRR Memorial Hermann
CollaboratorOTHER
University of Montana
CollaboratorOTHER
Baylor College of Medicine
CollaboratorOTHER
The University of Texas Health Science Center, Houston
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* have a traumatic spinal cord injury * be at least one year post injury * be able to speak and read English (to participate in the group intervention and complete study questionnaires in English). * have access to a phone, an email account, and a computer and high-speed Internet connection that meets minimum SL computing requirements.

Exclusion criteria

* have a cognitive impairment that significantly limits their ability to give informed consent, participate in the intervention, or complete study assessments as determined by an inability to correctly answer questions on a comprehension of consent questionnaire * have a significant visual or hearing impairment that would prohibit their ability to participate in the virtual intervention * report active suicidality * live in institutions. Individuals living in community-based group and adult foster homes will be invited to participate.

Design outcomes

Primary

MeasureTime frameDescription
Self-esteem as assessed by the Rosenberg Self-Esteem ScaleBaselineThe effect of the Zest intervention on self-esteem as assessed by the Rosenberg Self-Esteem Scale. This is a 10-item scale with scores ranging from 10-40 with higher scores indicating higher self-esteem.
Depression as assessed by the Patient Health Questionnaire-9 (PHQ-9)BaselineThe effect of the Zest intervention on depression as assessed by the Patient Health Questionnaire-9 (PHQ-9). This is a 9-item scale with scores ranging from 0-27 with higher scores indicating more severe depression.
Life satisfaction as assessed by the Satisfaction with Life ScaleBaselineThe effect of the Zest intervention on life satisfaction as assessed by the Satisfaction with Life Scale. This is a 5-item scale with scores ranging from 5-35 with higher scores indicating greater satisfaction with life.

Secondary

MeasureTime frameDescription
Self-efficacy as assessed by the Generalized Self-Efficacy ScaleBaselineThe effect of the Zest intervention on self-efficacy as assessed by the Generalized Self-Efficacy Scale. This is a 10-item scale with scores ranging from 10-40 with higher scores indicating higher self-efficacy.
Social connectedness as assessed by the Medical Outcomes Study Social Support Scale, Emotional/Informational Support subscale.BaselineThe effect of the Zest intervention on social connectedness as assessed by the Medical Outcomes Study Social Support Scale, Emotional/Informational subscale. This is an 8-item scale in which scores for each item are averaged. Scores are converted to a 0-100 scale with higher scores indicating more support and, therefore, social connectedness.
Perceived stress as assessed the by Perceived Stress ScaleBaselineThe effect of the Zest intervention on perceived stress as assessed by the Perceived Stress Scale. This is a 10-item scale with scores ranging from 0-40 with higher scores indicating more perceived stress.

Countries

United States

Outcome results

None listed

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