- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07588451
Effectiveness of a Brief Gratitude Writing Intervention on State Optimism, State Gratitude, and Psychological Distress
May 10, 2026 updated by: Kainat Safdar, Kinnaird College for Women
Effectiveness of a Brief Gratitude Writing Intervention on State Optimism, State Gratitude, and Psychological Distress Among Female University Students
The goal of the study is to investigate the effectiveness of brief writing interventions on state optimism, state gratitude and psychological distress among female university students.
There are three groups; gratitude writing group where participants are required to write about the things they are grateful for, expressive writing group where participants are required to write about their deepest feelings and thoughts from last week and a control group where participants just write about the tasks they completed in the past week.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
96
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Kainat Safdar
- Phone Number: +923164684767
- Email: kainat.safder@gmail.com
Study Locations
-
-
Punjab Province
-
Lahore, Punjab Province, Pakistan, 54000
- Kinnaird College For Women University
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Female undergraduate students
- Students scoring mild to moderate distress on Kessler Psychological Distress scale
Exclusion Criteria:
- Female university students enrolled in psychology programs
- Students with physical disability
- Students who are already in therapy
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Gratitude Writing
Participants write about the things they are grateful.
They are given a total of 10 mins with no language or structural limit or restriction for the writing.
|
Participants write the things they are grateful and thankful in their life for.
It could be anything they want to write about for a period of 10 mins.
They can write it in the language of their own choice and in what ever format they prefer.
|
|
Active Comparator: Expressive Writing
Participants are asked to write about their deepest thoughts and feelings from the past week for a period of 10 mins without any language or structure limit or restriction.
|
Participants write about their deepest feelings and thoughts from the past week.
They are given 10 mins to write.
They can write in language of their own choice and in any format they prefer.
|
|
Sham Comparator: Control
The participants were asked to write about the tasks they completed in the past week for 10 mins without any language of structure limit or restriction
|
Participants are asked to write about the tasks they have completed in the past week in 10 mins.
They can write in the language of their choice and in any format they prefer
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
State Optimism measured by State Optimism Measure
Time Frame: Baseline (pre-intervention) and immediately after the intervention
|
Change in state optimism assessed using the State Optimism Measure.
Higher scores indicate greater levels of state optimism.
|
Baseline (pre-intervention) and immediately after the intervention
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
State gratitude measured by the Gratitude Adjective Checklist
Time Frame: Baseline (pre-intervention) and immediately after the intervention
|
Change in state gratitude assessed using the Gratitude Adjective Checklist.
Higher scores indicate greater levels of state gratitude.
|
Baseline (pre-intervention) and immediately after the intervention
|
|
Psychological distress measured by the Kessler Psychological Distress Scale (K10)
Time Frame: Baseline (pre-intervention) and immediately after the intervention
|
Change in psychological distress assessed using the Kessler Psychological Distress Scale (K10).
Total scores range from 10 to 50, with higher scores indicating greater psychological distress.
|
Baseline (pre-intervention) and immediately after the intervention
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
June 20, 2026
Primary Completion (Estimated)
August 1, 2026
Study Completion (Estimated)
August 1, 2026
Study Registration Dates
First Submitted
April 30, 2026
First Submitted That Met QC Criteria
May 10, 2026
First Posted (Actual)
May 14, 2026
Study Record Updates
Last Update Posted (Actual)
May 14, 2026
Last Update Submitted That Met QC Criteria
May 10, 2026
Last Verified
May 1, 2026
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 46hv4152kbj2451
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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