NCT05824572 · Dartmouth-Hitchcock Medical Center
The Effect of Clinic Visit Audio Recordings for Self-management in Older Adults
(REPLAY)
What this study is about
The objective of this study is to conduct a multisite trial evaluating the impact of adding an audio recording of clinic visits (AUDIO) to usual care in older adults with multimorbidity, including diabetes, compared to After Visit Summary (AVS) alone (Usual Care; UC).
View original scientific description
The objective of this study is to conduct a multisite trial evaluating the impact of adding an audio recording of clinic visits (AUDIO) to usual care in older adults with multimorbidity, including diabetes, compared to After Visit Summary (AVS) alone (Usual Care; UC).
Who can participate
This study lists these criteria on ClinicalTrials.gov. A study coordinator reviews eligibility during screening — this page does not determine whether you qualify.
Inclusion criteria
- Patients who are ≥ 65 years;
- Patients with multimorbidity (i.e. patient has diabetes and one or more chronic conditions including: arthritis, asthma, atrial fibrillation, cancer, chronic obstructive pulmonary disease, heart disease, depression, heart failure, hypertension, osteoporosis, kidney disease and stroke);
- Have had two or more clinic visits in the previous 12 months;
- Plan on receiving ongoing care at the clinic for the subsequent 12 months;
- Do not have any vision or hearing problems that cannot be corrected;
- Have not recorded a clinic visit for personal use i the past 6 months.
Exclusion criteria
- Without capacity to consent to the project;
- With schizophrenia and other psychotic disorders, substance-use disorders, uncorrectable hearing or visual impairment or a six item screener (SIS) cognitive function score ≤ 4;
- Living in skilled nursing homes or hospice;
- Patients who have audio- recorded a clinic visit for their personal use in the previous six months;
- Patients who do not speak English or Spanish;
- Patients who lack internet access;
- Patients who (a) do not have access to a personal email, (b) do not have an email address shared with a family member or patient-identified caregiver, and (c) are not interested in creating an email account between the time they are first contacted by the study team to the time that the study team requires an email address to initiate the online recording software registration. Clinician participants: Inclusion criteria:
- Licensed clinician (MD including clinician residents at Dartmouth Health locations, DO, APRN, NP, PA)
- Are based at the study clinic;
- Who treat adult patients. Exclusion criteria:
- Are trainees, e.g., fellows, medical students or residents, with the exception of clinician residents at Dartmouth Health;
- Commonly audio or video record clinic visits for patient's personal use.
Where
- Manchester, New Hampshire
- Nashville, Tennessee
- Galveston, Texas
Frequently asked questions
What is a clinical trial?
A clinical trial is a research study that tests new medical treatments, drugs, devices, or procedures to determine their safety and effectiveness. Trials are carefully designed and monitored to protect participants while advancing medical knowledge.
Is it safe to participate?
Clinical trials follow strict safety guidelines and ethical standards. Trials must be reviewed and approved, and participants are closely monitored by medical professionals throughout the study. You can withdraw at any time if you choose.
Will I be compensated?
Many clinical trials offer compensation for your time, travel expenses, and inconvenience. The specific compensation varies by study and will be discussed during the screening process. All study-related medical care is typically provided at no cost to participants.
Will I receive a placebo instead of treatment?
When effective treatment exists, participants typically receive either the standard treatment plus the study intervention, or the standard treatment plus placebo. You would not be denied effective care. Placebos are primarily used when no proven treatment is available, or in addition to standard care. Your trial consent form will clearly explain what treatments you may receive.
Can I leave a trial if I change my mind?
Absolutely. Participation in clinical trials is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty or loss of benefits to which you are otherwise entitled.
How long does a clinical trial last?
Trial duration varies widely depending on the study design and purpose. Some trials last just a few weeks, while others may continue for months or years. The study coordinator will provide specific timeline information during your screening call.
Data: ClinicalTrials.gov · synced Jul 14, 2025 · Source of record for eligibility and locations