Skip to content

Efficacy of short message services on treatment adherence, severity of depression and spiritual health in depressed patients

A clinical trial for comparison the effects of sending one-way short message, interactive short message and not sending any message on adherence to medication, depression, and spiritual health among patients with major depression

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015091323998N1
Enrollment
90
Registered
2015-10-25
Start date
2015-10-22
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

Condition 1: Depressive episode. Condition 2: Depressive episode. Moderate depressive episode Severe depressive episode

Interventions

Intervention 1: Control group: The patients in control group will not be received any short messages. Intervention 2: Non- interactive message group: In this group the patients receive every day hopef
Control group: The patients in control group will not be received any short messages.
Non- interactive message group: In this group the patients receive every day hopeful message derived from traditions and elite, and tips about side effects, percussion, and medication reminder for 6 w
Interactive message group: In this group the patients receive every day hopeful message derived traditions and elite, and tips about side effects, percussion, and medication reminder, to which should

Sponsors

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

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: major depression according to diagnosis of a psychiatrist and DSM-IV-TR criteria; being literate; being able to work with cell phone and reading and writing a text message Exclusion criteria: refusing to participate in the study and lack of cooperation during the intervention

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Spiritual well- being. Timepoint: The beginning and end of the study. Method of measurement: Paloutzian and Ellison spiritual well-being scale.;Depression severity. Timepoint: The beginning and end of the study. Method of measurement: Beck Depression Inventory (21 question).;Treatment adherence. Timepoint: The beginning and end of the study. Method of measurement: Treatment adherence self- made questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNajme Shahinfard

Virtual School, Tehran University of Medical Sciences

shahinfardn@yahoo.com+98 21 8897 8088

Outcome results

None listed

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