- ICH GCP
- Registr klinických studií v USA
- Klinická studie NCT01334398
A Health & Wellness Intervention for Individuals With Traumatic Brain Injury (TBI)
A Health & Wellness Intervention for Individuals With Traumatic Brain Injury
Přehled studie
Postavení
Podmínky
Intervence / Léčba
Detailní popis
Health promotion in the general population and in disability groups, such as individuals with TBI, has been identified in recent decades as a specific need by the Surgeon General, the U.S. Department of Health and Human Services Healthy People 2010, the NIDRR Rehabilitation Research and Training Center (RRTC) on Health and Wellness and the Centers for Disease Control and Prevention (CDC). Additionally, decreased quality of life and increased health-related secondary conditions in TBI supports the need for health and wellness promotion. A number of health and wellness programs have been developed for specific disabled populations, with a few providing evidence for efficacy; however, no evidence based program designed to meet the unique needs of individuals with TBI has been identified. This proposal responds to the NIDRR Long Range Plan and the Healthy People 2010 call for further research in health promotion to improve quality of life, decrease disability, and eliminate disparities in health within disability populations, specifically those individuals with TBI.
The primary goal of the proposed study is to evaluate the efficacy of a replicable community-based group intervention, designed to address both general wellness and specific TBI health-related issues. Emphasis is placed on goal setting to develop healthy living habits, utilize problem solving strategies, learn means of maintaining progress and set new goals. Facilitators will utilize approaches aimed at maximizing participant self-efficacy, reducing barriers to health promotion, and developing personal resources. A randomized wait-list control group design will be used to evaluate the efficacy of the intervention.
It is hypothesized that individuals with TBI who participate in the intervention group will report increased health promoting behaviors, health related self-efficacy, health-related quality of life, level of participation, and greater perceived wellness and satisfaction with life, than the control group. Intervention group members are expected to attain individualized health and wellness goals, and maintain gains on follow-up at six months. Findings from this study will advance knowledge regarding health and wellness intervention for individuals with TBI, and may clarify areas of future research.
Typ studie
Zápis (Aktuální)
Kontakty a umístění
Studijní místa
-
-
Colorado
-
Denver, Colorado, Spojené státy, 80220
- VA ECHCS
-
-
Kritéria účasti
Kritéria způsobilosti
Věk způsobilý ke studiu
Přijímá zdravé dobrovolníky
Pohlaví způsobilá ke studiu
Metoda odběru vzorků
Studijní populace
Popis
Inclusion Criteria:
individuals will be included in the study if they meet the following criteria:
- history of TBI as defined as damage to brain tissue caused by an external mechanical force as evidenced by loss of consciousness or post traumatic amnesia (PTA) due to brain trauma or by objective neurological findings that can be reasonably attributed to TBI on physical examination or mental status examination.
- received inpatient or outpatient rehabilitation, or an evaluation related to their TBI;
- are classified as moderate to severe TBI based on a TBI medical/professional evaluation;
- are at least one year post-injury;
- are 18 years of age or older at the time of the study;
- function at Rancho Los Amigo Level of Cognitive Functioning Level of 6 or above, based on current interview with participant and family member/identified resource person
- have adequate receptive and expressive communication skills functional for group participation (score >5 on the Comprehension and Expression items of the Functional Independence Measure (FIM) based on current interview);
- have sufficient recall of day-to-day events for learning in the group setting, based on screening interview with family member or identified resource person;
- have the ability to participate in ongoing group sessions with no documented or reported medical or neurological conditions (e.g. upcoming hospitalizations, uncontrolled seizures), behavioral concerns (e.g. frustration tolerance, behavioral/anger control,) or other issues that preclude group participation;
- be English speaking in order to complete study measures (if the intervention is proven efficacious, future studies would be needed with non-English speaking participants);
- provide informed consent to participate.
Exclusion Criteria:
- Failure to meet inclusion criteria
- Failure to provide informed consent as evidenced by inability to respond to the above stated questions
Studijní plán
Jak je studie koncipována?
Detaily designu
Kohorty a intervence
Skupina / kohorta |
Intervence / Léčba |
---|---|
Initial Treatment Group
|
The specific content of the intervention was adapted from four existing evidence-based interventions: (1) "Healthy Lifestyles for People with Disabilities," (2) Promoting Wellness for Women with MS," (3) "Living Well with Disability," and (4) "Social Skills and TBI: A Workbook for Group Treatment."
|
Deferred Treatment Group
|
The specific content of the intervention was adapted from four existing evidence-based interventions: (1) "Healthy Lifestyles for People with Disabilities," (2) Promoting Wellness for Women with MS," (3) "Living Well with Disability," and (4) "Social Skills and TBI: A Workbook for Group Treatment."
|
Co je měření studie?
Primární výstupní opatření
Měření výsledku |
Časové okno |
---|---|
Health Promoting Lifestyle Profile-II
Časové okno: Baseline and Follow-up
|
Baseline and Follow-up
|
Spolupracovníci a vyšetřovatelé
Spolupracovníci
Vyšetřovatelé
- Vrchní vyšetřovatel: Lisa Brenner, Ph.D., VA VISN 19, ECHCS
- Vrchní vyšetřovatel: Cynthia Braden (nee Dahlberg), MA, Craig Hospital
Termíny studijních záznamů
Hlavní termíny studia
Začátek studia
Primární dokončení (Aktuální)
Dokončení studie (Aktuální)
Termíny zápisu do studia
První předloženo
První předloženo, které splnilo kritéria kontroly kvality
První zveřejněno (Odhad)
Aktualizace studijních záznamů
Poslední zveřejněná aktualizace (Odhad)
Odeslaná poslední aktualizace, která splnila kritéria kontroly kvality
Naposledy ověřeno
Více informací
Termíny související s touto studií
Klíčová slova
Další relevantní podmínky MeSH
Další identifikační čísla studie
- 07-1146
- H133A070022 (Jiné číslo grantu/financování: NIDRR)
Tyto informace byly beze změn načteny přímo z webu clinicaltrials.gov. Máte-li jakékoli požadavky na změnu, odstranění nebo aktualizaci podrobností studie, kontaktujte prosím register@clinicaltrials.gov. Jakmile bude změna implementována na clinicaltrials.gov, bude automaticky aktualizována i na našem webu .
Klinické studie na Traumatické zranění mozku
-
The Hong Kong Polytechnic UniversityDokončenoMrtvice | Rozhraní Brain ComputerHongkong
-
Wright State UniversityZatím nenabírámeBolest hlavy | Bolest hlavy vyvolaná chladem | Brain Freeze | Cephalgie vyvolaná chladem
-
Neurolutions, Inc.Washington University School of MedicineZatím nenabírámeMrtvice | Hemiparéza | Spasticita jako pokračování mrtvice | Rozhraní Brain ComputerSpojené státy
Klinické studie na Health & Wellness
-
McGill UniversityDokončenoKardiovaskulární onemocnění
-
University of FloridaRTI International; Centers for Medicare and Medicaid Services; Econometrica,...DokončenoChronická duševní nemoc | Chronická fyzická nemocSpojené státy
-
M.D. Anderson Cancer CenterNational Institute on Drug Abuse (NIDA)Dokončeno
-
University of Texas at AustinDokončenoZdravý | Chronická bolest | Stres, psychologickýSpojené státy
-
Bournemouth UniversityRoyal Bournemouth and Christchurch Hospitals NHS Foundation Trust; Oomph! Wellness a další spolupracovníciStaženoSyndrom křehkých starších lidí | Křehkost | Sedavé chování | Nemoc způsobená životním stylem | Životní styl, Sedavý
-
Mayo ClinicDokončenoZánětlivá onemocnění střev | Crohnova nemoc | Ulcerózní kolitidaSpojené státy
-
University of Texas at AustinDokončeno
-
University of Texas at AustinDokončenoZdravý | Revmatoidní artritida | Chronická bolest | Stres | PsychologickýSpojené státy
-
Federal University of São PauloFundação de Amparo à Pesquisa do Estado de São PauloDokončenoObezita | SchizofrenieBrazílie
-
The University of Texas Health Science Center at...National Cancer Institute (NCI); Wake Forest University Health Sciences; Arizona... a další spolupracovníciNáborDeprese | Zánět | Rakovina | Únava | Úzkost | Poruchy spánkuSpojené státy