Skip to content

A Health and Wellness Lifestyle Program to Support Community-Dwelling Persons With Traumatic Brain Injury

A Health and Wellness Lifestyle Program to Support Community-Dwelling Persons With Traumatic Brain Injury (TBI) and Their Caregivers: In-House Research Project, Objective 2

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04288258
Acronym
POWERS-TBI
Enrollment
62
Registered
2020-02-28
Start date
2020-04-01
Completion date
2023-10-01
Last updated
2023-10-31

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

Conditions

Traumatic Brain Injury

Brief summary

To evaluate the efficacy of an adapted telehealth-based, health and wellness lifestyle program on promoting healthy lifestyle behaviors and improving health outcomes.

Detailed description

The purpose of this study is to evaluate the efficacy of an adapted telehealth-based, health and wellness lifestyle program (POWERS-TBI) on promoting healthy lifestyle behaviors and improving self-efficacy for healthy activities such as amount of physical activity, dietary/food intake, mental stimulation and activity, substance use, mindfulness/spirituality, social relationships, and/or leisure activities among persons with TBI and their caregivers. The treatment program will be delivered via the internet, along with ongoing telephone health coaching calls designed to motivate, problem-solve challenges, reinforce skills learned, and prevent relapse. The goals are to evaluate the impact of the treatment program on improving health outcomes for people with TBI. The investigators plan to accomplish this by evaluating the impact of the program using a case-control crossover design.

Interventions

BEHAVIORALTelehealth-Based Health and Wellness Program (POWERS-TBI)

The treatment program is interactive and will be delivered via the internet, along with ongoing telephone health coaching calls designed to motivate, problem-solve challenges, reinforce skills learned, and prevent relapse.

Sponsors

University of Alabama at Birmingham
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

case-control crossover

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* age 19 years or older * sustained a TBI * at least 6-months or greater out from injury * willing to work on one or more health goals among any of the following areas of focus (e.g., health knowledge, physical activity/exercise, dietary intake/nutrition, stress management, mental activity/stimulation, social ' relationships, leisure, sleep, mindfulness/spirituality, substance use) * able to potentially participate in physical activity or alter dietary intake, if that is a potential health goal (e.g., no medical contraindication given by their doctor) * not currently enrolled in a health and wellness program or research study involving a health/wellness program or intervention * indicates a potential health goal to lose weight and does not independently prepare their own meals, cook, grocery shop, but has a caregiver defined by providing some type of ongoing support (emotional or instrumental) who is willing to participate as a study partner during the intervention condition * has access to a telephone * has regular access to the internet from a computer or laptop * not pregnant (due to the effect on engaging in certain health promoting behaviors such as weight loss) * does not have a significant psychiatric disorder, such as schizophrenia or bipolar disorder (those with depression or anxiety will not be excluded)

Exclusion criteria

* non-English speaking * difficulty hearing * significant problems with communication

Design outcomes

Primary

MeasureTime frameDescription
Health Promoting Lifestyle Profile IIUp to 13 monthsHPLP-II; Total scores and subscale scores are summed and divided by number of items on each scale respectively for an average, with higher scores indicating greater lifestyle behaviors

Secondary

MeasureTime frameDescription
Zarit Burden ScaleUp to 13 monthsZBS: Scores are summed (ranges 0 to 48) for a total scores, higher scores are indicative of greater burden
Sociodemographic CharacteristicsUp to 13 monthsNo abbreviation: Frequencies, summed total, or averages are reported to characterize the sample
Barriers to Physical Activity and Disability SurveyUp to 13 monthsBPADS: Response choices (yes/no) for 31 items are summarized; 3 items are open-ended, higher scores indicate greater barriers
Social Support and Exercise Support for Eating and Physical Activity HabitsUp to 13 monthsSSES: Subscale scores are obtained for exercise support (ranging from 10 for friends and 10 for family to 80 for friends and 80 for family); higher scores indicate greater support
Stages of Change Readiness and Treatment Engagement ScaleUp to 13 monthsSOCRATES: Items are summed and averaged across each subscale: Recognition scores range from 7-35; Ambivalence scores range from 4-20; Taking Steps scale range from 8-40: Higher scores indicate greater motivation
Barriers to Health Activities among Disabled Persons scaleUp to 13 monthsBHADP: Ratings are summed across each item for how interfering they are with health promotion (range of possible scores 18 to 72)
Fatigue Severity ScaleUp to 13 monthsFSS: Scores range from 9 to 63 with higher scores indicating greater fatigue
Bodily Pain IndexUp to 13 monthsBPI: Scores for the Interference scale are summed and average for a mean (range 0 to 70) with higher scores indicating greater pain interference
Craig Handicap Assessment Reporting Technique short formUp to 13 monthsCHARTsf: Suscales scores are summed and averaged for respective scales with higher scores indicating greater community integration
Perceived Wellness SurveyUp to 13 monthsPWS: A total score and subscale scores are calculated with a formula and range between 36 to 316 and average with higher scores indicating greater personal wellness
Patient Health Questionnaire-9 ItemUp to 13 monthsPHQ-9: Scores are summed and range from 0 to 27, higher scores indicate greater depressive symptomatology

Countries

United States

Outcome results

None listed

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