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Behavioural Intervention
Internet-Delivered Psychotherapy for Depression
N/A
Recruiting
Led By Julia Kirkham, MD
Research Sponsored by University of Calgary
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline, mid-point (4-weeks) and after completing the program (8-weeks).
Awards & highlights
Study Summary
This trial will develop, adapt and evaluate a new internet-delivered psychotherapy option (Ger-iPST) to improve access to psychotherapy for older adults with depression.
Who is the study for?
This trial is for people aged 65 or older who feel depressed, have a PHQ-9 score over 5, speak English, and can access the internet. It's not for those with immediate safety concerns like suicidal thoughts, psychotic symptoms, moderate cognitive issues (MoCA < 21), or those already in psychotherapy.Check my eligibility
What is being tested?
The study tests Ger-iPST—an online therapy program designed to help older adults with depression. Participants will do weekly web-based modules and homework through OPTT and get feedback from clinicians plus support calls for technical help.See study design
What are the potential side effects?
Since this is a psychotherapy trial involving counseling rather than medication, typical medical side effects are not expected. However, participants may experience emotional discomfort while discussing personal issues during therapy.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline, mid-point (4-weeks) and after completing the program (8-weeks).
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline, mid-point (4-weeks) and after completing the program (8-weeks).
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Measure the effectiveness for symptoms of depression in older adults.
Secondary outcome measures
Examine implementation outcomes - Anxiety symptoms.
Examine implementation outcomes - Disability Assessment.
Examine implementation outcomes - Quality of life.
+2 moreTrial Design
1Treatment groups
Experimental Treatment
Group I: Ger-iPSTExperimental Treatment1 Intervention
Prospective participants will be contacted by telephone to confirm eligibility, explain the study protocol, and obtain informed consent. An in-person or videoconference assessment will be used to administer baseline PHQ-9 to confirm enrolment criteria and will be asked questionnaire to gather demographic information. Participants will then be provided with an email link to access the Online Psycho Therapy Tool (OPTT). PHQ-9 will be collected again at the mid-point (4 weeks) and after completing the program through OPTT. Caregivers will be invited to assist the participant if required in completing Ger-iPST modules, and weekly telephone support calls by a research assistant will be provided to assist with any difficulty navigating technical aspects of the Ger-iPST platform.
Find a Location
Who is running the clinical trial?
University of CalgaryLead Sponsor
792 Previous Clinical Trials
869,141 Total Patients Enrolled
Hotchkiss Brain Institute, University of CalgaryOTHER
11 Previous Clinical Trials
2,419 Total Patients Enrolled
Julia Kirkham, MDPrincipal InvestigatorUniversity of Calgary
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I speak English.I am currently undergoing psychotherapy.I am feeling depressed with a PHQ-9 score above 5.I am 65 years old or older.
Research Study Groups:
This trial has the following groups:- Group 1: Ger-iPST
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Are there openings in this research study for new participants?
"The clinical trial is presently enrolling patients, as per the information available on clinicaltrials.gov. This study was initially advertised on January 1st of 2023 and its most recent update can be found from February 21st of that year."
Answered by AI
How many individuals are presently contributing to this clinical experiment?
"Affirmative. As per the clinicaltrials.gov database, this medical trial is actively acquiring participants, with a first post date of January 1st 2023 and an updates on February 21st 2023. There are 13 spots available at one site."
Answered by AI
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