Evaluation of the effectiveness of spiritual intervention on pain intensity and quality of life in end-of-life patients

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20210513051282N1

Enrollment

Registered

2021-07-11

Start date

2021-05-22

Completion date

Unknown

Last updated

2021-08-30

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

Conditions

Reducing pain and quality of life.

Interventions

Intervention 1: Intervention group: Spiritual Care Content is based on the titles of Richards and Bergin Spiritual Intervention Sessions in six 60-minute sessions over four months. Intervention 2: Con

Eligibility

Sex/Gender

All

Age

16 Years to No maximum

Inclusion criteria

Inclusion criteria: According to medical parameters, they are less than 6 months old Has at least a diploma Age 19 years and above Believes in the Shia religion Awareness above 8

Exclusion criteria

Exclusion criteria: Decrease the patient's level of consciousness to less than 8 during interventions for 4 consecutive days

Design outcomes

Primary

Measure	Time frame
Reduce pain. Timepoint: Before the intervention and two weeks after the intervention. Method of measurement: Von Korf Pain Intensity Questionnaire.;Quality of Life. Timepoint: Von Korf Pain Intensity Questionnaire. Method of measurement: Quality of Life Questionnaire.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSeyed Mahmoud Tabatabaei

Mashhad University of Medical Sciences

tabanet@um.ac.ir+98 51 3841 5777

Outcome results

None listed

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