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Effect of supportive nursing care on anxiety, self-esteem and Satisfaction of patients receiving electroconvulsive therapy: A randomized controlled clinical trial

Effect of supportive nursing care on anxiety, self-esteem and Satisfaction of patients receiving electroconvulsive therapy: A randomized controlled clinical trial

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT201306036834N6
Enrollment
Unknown
Registered
2013-07-23
Start date
2013-07-16
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Psychiatric patients receiving ECT. Schizophrenia, Maniaic episode, Bipolar affective disorder, Depressive episode, Recurrent depressive disorder

Interventions

Intervention 1: Intervention group: Firstly, the pre-test will be done. Intervention group, during the electroconvulsive therapy proceedings (minimum 4 sessions) will be receiving supportive cares fro
Intervention group: Firstly, the pre-test will be done. Intervention group, during the electroconvulsive therapy proceedings (minimum 4 sessions) will be receiving supportive cares from nurses. Then,
Control group: Firstly, the pre-test will be done. Control group, during the electroconvulsive therapy proceedings (minimum 4 sessions) will be receiving routine interventions from nurses. Then, the p

Sponsors

Vice chancellor for research, Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: Eligibility criteria for participants: Patients receiving ECT and are aged 18 years and older; ability to read and write; lack of physical disease lead to cognitive impairment; lack of perception disorders and impairment in reality test; lack of anxiety disorders; and lack of bipolar disorder with high self-esteem. Exclusion criteria for participants: Patients who are in acute phase of psychosis; patients who are refusing to continue to participate in the study; patients who are receiving less than 4 sessions of ECT.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Anxiety. Timepoint: Before intervention and six hours after finishing intervention. Method of measurement: Spielberger's Anxiety Questionnaire.;Self-esteem. Timepoint: Before intervention and six hours after finishing intervention. Method of measurement: Rosenberg's Self-esteem Questionnaire.;Satisfaction. Timepoint: Before intervention and six hours after finishing intervention. Method of measurement: Webster Satisfaction Questionnaire.

Countries

Iran (Islamic Republic of)

Outcome results

None listed

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