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Influence of spiritual support program on quality-of-life of stroke survivors post substance overdose: A randomized controlled trial

Influence of spiritual support program on quality-of-life of stroke survivors post substance overdose: A randomized controlled trial

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
TCTR
Registry ID
TCTR20250204005
Enrollment
90
Registered
2025-02-04
Start date
2023-06-15
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

quality-of-life of stroke survivors post substance overdose Keywords: Drug intoxication, Spirituality, Quality of life, Stroke, Patient

Interventions

Prior to the intervention, both the control and intervention groups completed the demographic questionnaire and the SS-QoL. Participants were assured of the confidentiality of their responses. Followi
spiritual well-being. Session 1 focused on establishing supportive systems, where patients received instruction about the study&#039
s purpose and spiritual care. This session aimed to build trust, empathy, and honesty between the nurse and the patient, provide psychological support, cultivate hope and inner strength, and encourage
religious practices by assisting them in exploring the meaning of life, performing religious rituals, and seeking guidance from religious authorities. Session 3 implemented supportive systems by encou
spiritual support program,Control Group

Sponsors

Urmia University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria were as follow: (a) Willingness to Participate: All participants must voluntarily agree to take part in the study. (b) Signed Consent: Participants must provide written consent, indicating their understanding and agreement to the study's procedures and potential risks. (c) Ischemic Stroke Diagnosis: Participants must have a confirmed diagnosis of ischemic stroke. (d) Self-Care Ability: Participants must be capable of performing basic self-care tasks independently. (e) Time Since Stroke Onset: Participants must be at least 48 hours post-stroke onset. (f) Age Range: Participants must be between 18 and 60 years of age. (g) History of Drug Stimulant Use: Participants must have a history of using drug stimulants.

Exclusion criteria

Exclusion criteria: Exclusions were severe visual or hearing impairments and refusal to participate. If a selected participant declined, the next person was randomly selected to participate. The participants had been using various substances, including opioids, stimulants, and benzodiazepines, for an average of 3 years prior to their stroke event. None of the participants had regularly practiced yoga or other spiritual/mindfulness practices before the study.

Design outcomes

Primary

MeasureTime frame
quality-of-life of stroke survivors post substance overdose 1 month Stroke-Specific Quality of Life (SS-QoL) scale

Secondary

MeasureTime frame
N/A N/A N/A

Countries

Iran

Contacts

Public ContactRasoul Goli

Urmia University of Medical Sciences, Iran

Rasoulgoli94@gmail.com9148854057

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Apr 4, 2026