NCT06827093Completed
Dyadic Interventions to Boost Quality of Life Among Stroke Survivors and Care Partners in Pakistan.
Augmented Dyadic Interventions to Boost Quality of Life Among Stroke Survivors and Care Partners in Pakistan.
Source: ClinicalTrials.gov · Last updated 14 Feb 2025
Brief summary (registry, in English)
This study (RCTs) will be conducted on stroke survivors and their care partners after discharge from the hospital. The study will aim to evaluate the impact of augmented dyadic intervention on the quality of life of stroke survivors and caregiver burden. A randomized control trial with a parallel group design will be used for the study. The design used for the current study will be single-blind, randomized controlled trials with repeated measures. Each group will include 196 subjects (98 stroke survivors and 98 care partners). The total number of individuals will be 392, including 196 stroke survivors and 196 care partners. Stroke survivors will have an age range of 18-75 years and both genders with a confirmed diagnosis of stroke. The goal of this study will be to rehabilitate patients with disability, there is a dire need for dyad interventions to support and train stroke care partners by providing education, counselling, emotional support and access to health services. The hypothesis of this (RCTs )is that there is no relationship between stress and quality of life for improvement in quality of life through dyadic intervention.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 392 (actual)
- First submitted
- 12 Aug 2024
- Start date
- 1 Oct 2021
- Primary completion date
- 1 Sept 2023
- Lead sponsor
- Zhengzhou University
- Diseases
- Stroke
- NCT number
- NCT06827093
What you commit to
- Study type: Interventional
- Participants enrolled: 392
- From 1 Oct 2021 to the primary completion date, 1 Sept 2023
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- Acute illness (i.e., dementia, advanced cancer, hepatic or renal failure or fractured lower extremity)
- Preexisting diseases before stroke
- Post-invasive procedural strokes like CABG, angiography and post-operative stroke
- Global aphasia and/or being unable to communicate. Dementia on the Mini-Mental State Examination (of \<22) (due to inability to directly communicate) 26,27
- History of ongoing psychoactive substance abuse, terminal illnesses like renal failure or end-stage cancer
- The presence of psychiatric morbidity before and after stroke, which specifically includes manic disorders, schizophrenia
Age
- 1\. having an age greater than 80 years 2. Acute illness
Other
- Life expectancy of 6 months or less.
- \-
Who the study is looking for
- The study includes stroke survivors:
- Having an age range of 18-75 years with a confirmed diagnosis of stroke (confirmed by a neurologist with radiological evidence by either CT scan and/or MRI) and meeting the following eligibility criteria was required. 26
- Having a diagnosis of stroke More than 15 days
- Stable, non-fluctuating stroke with no acute, ongoing neurological
- No preexisting disability before stroke (defined by mRS =0).
- Independent in daily living activities before the stroke
- Expected to return home with residual disability
- While the inclusion criteria for care partners was an identified primary care partner greater than 18 years of age,
- Able to speak
- Urdu speaker
- Care partners include aphasic patients and demented patients.
- No significant physical or psychological disability
- Be willing and able to provide support to patients after discharge
Age in the registry: 18 years to 70 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Dr.Nazia Coordinator of this site? Confirm its status | Zhengzhou | China | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.