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Guided Imagery for Stroke Survivor-Caregiver Dyads with Psycholoogical Distress: A Randomized Clinical Trial

Guided Imagery for Stroke Survivor-Caregiver Dyads with Psycholoogical Distress: A Randomized Clinical Trial

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200064877
Enrollment
Unknown
Registered
2022-10-20
Start date
2022-11-01
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

Stroke

Interventions

Control group:Usual care

Sponsors

Xi'an Jiaotong University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Inclusion criteria for patients: (1) Patients aged >=18 years with first-episode stroke meeting the diagnostic criteria of ''Chinese Guidelines for the Diagnosis and Treatment of Acute Ischemic Stroke 2018'' or ''Chinese Guidelines for the Diagnosis and Treatment of Cerebral Hemorrhage 2019'', and diagnosed with brain CT or MRI; (2) Accompanied by psychological distress, hospital anxiety Depression scale Depression scale (HADS-D) or anxiety subscale (HADS-A) >=8 points; (3) Stable condition, clear consciousness, GCS score >=13; (4) Proficient in using smart phones; (5) Sign informed consent. 2. Inclusion criteria for caregivers: (1) Family members >=18 years of age who provided the majority of unpaid care to the patient during and after hospitalization; (2) Accompanied by psychological distress, hospital anxiety Depression scale Depression scale (HADS-D) or anxiety subscale (HADS-A) >=8 points; (3) Proficient in using smart phones; (4) Sign informed consent.

Exclusion criteria

Exclusion criteria: 1. Previous or current mental illness; 2. Suffering from other serious diseases, such as heart disease, respiratory failure, malignant tumor, etc.; 3. Patients with cognitive impairment, language expression and communication impairment or hearing impairment; 4. Get involved in other research.

Design outcomes

Primary

MeasureTime frame
Psychological distress;

Secondary

MeasureTime frame
Illness perception;Co-rumination;Perceived social support;

Countries

China

Contacts

Public ContactLyu Aili
aili@mail.xjtu.edu.cn+86 13572498128

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026