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Communal Coping Intervention for Type 1 Diabetes

N/A
Recruiting
Led By Vicki Helgeson, Ph.D.
Research Sponsored by Carnegie Mellon University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Age 18 and over
Diagnosis of type 1 diabetes for at least one year
Must not have
Patient has a major chronic illness that affects daily life more than diabetes (e.g., currently undergoing treatment for cancer)
Non-English speakers
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline (from past 2 weeks), end of 2-week ecological momentary assessment (from past 2 weeks), 6-week followup (past 2 weeks)
Awards & highlights
No Placebo-Only Group

Summary

This trial tests a program that helps couples work together to manage type 1 diabetes. It targets couples where one partner has diabetes, aiming to improve their teamwork in handling the disease. The program includes setting shared goals and receiving regular support messages.

Who is the study for?
This trial is for adults over 18 with Type 1 Diabetes who've had it for at least a year. They must be married or living with a partner for the same duration, who's also willing to join the study. Participants need internet access and can't have other major illnesses overshadowing their diabetes. Non-English speakers and partners with diabetes are excluded.
What is being tested?
The trial is testing a new 'communal coping intervention' designed to help couples where one partner has Type 1 Diabetes work together better in managing the condition. It's about sharing the challenge of diabetes care between patient and partner through an online program.
What are the potential side effects?
Since this intervention involves psychological support rather than medication, traditional physical side effects aren't expected. However, participants may experience emotional discomfort or relationship dynamics changes as they adapt to new ways of coping together.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
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I am 18 years old or older.
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I have been diagnosed with type 1 diabetes for over a year.

Exclusion Criteria

You may be eligible for the trial if you check “No” for criteria below:
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I have a chronic illness more impactful than diabetes.
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I do not speak English.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline (from past 2 weeks), end of 2-week ecological momentary assessment (from past 2 weeks), 6-week followup (past 2 weeks)
This trial's timeline: 3 weeks for screening, Varies for treatment, and baseline (from past 2 weeks), end of 2-week ecological momentary assessment (from past 2 weeks), 6-week followup (past 2 weeks) for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
change in Self-Care Inventory from baseline to 6 weeks; higher score = better self-care; range 1-5; also change over ecological momentary assessment period
change in Type 1 Diabetes Distress Scale (Fisher et al., 2015) from baseline to 6 weeks; higher scores = more distress; range 1-6; also change over ecological momentary assessment period
Secondary study objectives
change in Center for Epidemiological Depression Scale from baseline to 6 weeks; higher numbers = more depressive symptoms; range = 0 to 30; also change over ecological momentary assessment period
change in Diener's life satisfaction scale from baseline to 6 weeks; higher numbers= more life satisfaction; range = 1-7; also change over ecological momentary assessment period
change in Quality of Marriage Index and intimacy subscale from Personal Assessment of Intimacy in Relationships from baseline to 6 weeks; higher numbers = better; range = 1 to 7; also change over ecological momentary assessment period
+2 more
Other study objectives
change in communal coping from baseline to 6 weeks; higher = more communal copingl; range = 0 to 10; also change over ecological momentary assessment period
change in diabetes communication from baseline to 6 weeks; higher numbers = more communication; range = 0 to 10; also change over ecological momentary assessment period
change in self-efficacy subscale from Multidimensional Diabetes Questionnaire from baseline to 6 weeks; higher numbers = greater efficacy; range = 0 to 100%; also change over ecological momentary assessment period
+1 more

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: Communal Coping InterventionExperimental Treatment1 Intervention
The intervention consists of a single session brief communal coping intervention followed by 7 days of intervention prompts delivered via text message to help couples generalize what they have learned into their daily life. There are 9 components to the intervention: 1. establishment of rapport 2. shared stressor recollection 3. communal coping education 4. application of appraisal to diabetes 5. we-statements to reframe diabetes as shared 6. facilitated discussion between couple members to identify each person's needs with active listening 7. collaborative implementation intentions 8. EMI text messaging for 7 days following intervention
Group II: Diabetes Education Attention ControlActive Control1 Intervention
These participants will receive diabetes education via a 15-20 minute videotape (as well the intervention group)
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Communal Coping Intervention
2019
N/A
~50

Research Highlights

Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.
Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
The primary treatment for Type 1 Diabetes (T1D) is insulin therapy, which involves administering exogenous insulin to compensate for the body's inability to produce insulin. This is essential for regulating blood glucose levels and preventing complications associated with hyperglycemia. Additionally, psychosocial interventions like the Communal Coping Intervention, which enhance shared appraisal of diabetes and increase patient-partner collaboration, are important. These interventions help improve treatment adherence and emotional well-being by creating a supportive environment, addressing both the psychological and social challenges of managing T1D. This holistic approach is vital for improving overall disease management and quality of life for T1D patients.
Short-term effects of coping skills training in school-age children with type 1 diabetes.Effects of Cognitive Behavioral Therapy-Based Intervention on Improving Glycaemic, Psychological, and Physiological Outcomes in Adult Patients With Diabetes Mellitus: A Meta-Analysis of Randomized Controlled Trials.An examination of the communal coping process in recently diagnosed diabetes.

Find a Location

Who is running the clinical trial?

Carnegie Mellon UniversityLead Sponsor
77 Previous Clinical Trials
539,822 Total Patients Enrolled
Juvenile Diabetes Research FoundationOTHER
234 Previous Clinical Trials
141,996 Total Patients Enrolled
Vicki Helgeson, Ph.D.Principal InvestigatorCarnegie Mellon University

Media Library

Communal Coping Intervention Clinical Trial Eligibility Overview. Trial Name: NCT05925556 — N/A
Type 1 Diabetes Research Study Groups: Communal Coping Intervention, Diabetes Education Attention Control
Type 1 Diabetes Clinical Trial 2023: Communal Coping Intervention Highlights & Side Effects. Trial Name: NCT05925556 — N/A
Communal Coping Intervention 2023 Treatment Timeline for Medical Study. Trial Name: NCT05925556 — N/A
~13 spots leftby Mar 2025