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Recruiting NCT07119710

Telehealth to Improve Quality of Life in Persons Living in Rural Texas

No phase Interventional Mental Health Issue Quality of Life

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Cognitive Behavioral Therapy, Cognitive Behavioral therapy with 2 check in calls.
Who it may be relevant to
Registry conditions: Mental Health Issue, Quality of Life. Basic parameters: 18 years — 110 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Improving Quality of Life in Persons Living in Rural Texas

Overview

The overarching goal of this project is to evaluate a current evidence-based practice, Cognitive Behavioral Therapy, for mental health conditions against Cognitive Behavioral Therapy plus two check-in calls a week for adults living in rural Texas.

Detailed description

This two-armed study, for adults living in rural Texas, aims to evaluate current evidence-based practice, Cognitive Behavioral Therapy, for mental health conditions against Cognitive Behavioral Therapy plus two check-in calls a weel.

Interventions

  • Behavioral Cognitive Behavioral Therapy
    Individual tele-therapy 12-16 weeks
  • Behavioral Cognitive Behavioral therapy with 2 check in calls
    Cognitive Behavioral therapy with 2 calls a week

Primary outcome measures

  • Pre-death grief (PG-12) [Time frame: Baseline Weekly before the intervention 1 Month following the intervention 3 Months following the intervention 6 months following the intervention]

Eligibility criteria

Inclusion criteria

  • family caregiver of person with all forms of dementia

Exclusion criteria

  • not in another clinical intervention

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Health services research

Study locations

United States · 1 center
  • Garrison Institute on Aging — Lubbock

Identifiers

NCT: NCT07119710 · TexasTechU3

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗