Between Paws and Affections: dog-assisted therapy for fibromyalgia
Official title: Between Paws and Affections: Impact of Dog Assisted Therapy on Pain, Emotional Symptoms, and Functioning in Fibromyalgia
Run by University of Minho · NCT07356206 · Data updated 2026-11-12
This project will test whether a 10-session dog-assisted therapy program, including weekly sessions and monthly booster relaxation sessions with dogs, helps reduce pain, anxiety, and depressive symptoms and improves function and quality of life in Portuguese adults with fibromyalgia followed at ULS Alto Ave.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 60 (estimated) |
| Sponsor | University of Minho Academic / other |
| Locations | 1 site (Guimarães) |
| Status | Recruiting |
| Started | January 22, 2026 |
| Main results expected | June 30, 2028 |
| Study ends | June 30, 2029 |
| Registry record updated | May 5, 2026 |
| Trial ID | NCT07356206 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults (18+) with a confirmed diagnosis of fibromyalgia who are followed at ULS Alto Ave, can read and write Portuguese, consent to participate, and are willing and able to attend the 10 group sessions and scheduled follow-up assessments.
✕Probably not a fit
Patients with dog allergy or marked fear of dogs, a history of oncological or confounding systemic/rheumatologic disease, decompensated psychiatric disorders, severe cognitive impairment, or those unable/unwilling to attend sessions are unlikely to benefit from this protocol.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This is a prospective, non-randomized clinical trial with a control group conducted at the Day Hospital of the Psychiatry and Mental Health Department of ULS Alto Ave. Participants receive group-based interventions: a 10-session dog-assisted therapy program (4 weekly DAT sessions plus 6 monthly guided-relaxation booster sessions with dogs) or an active control program providing identical psychoeducation and relaxation without dogs. Outcomes are measured immediately after the intervention, at 6 months, and at 12 months to examine both short-term effects and maintenance. The design follows up on a pilot of 34 women that showed initial benefits but partial erosion of gains at 6 months, motivating the prolonged protocol with boosters.
Why it matters
Potential benefit: If successful, the program could provide a non-drug option that reduces pain, anxiety, and depressive symptoms and helps maintain functional and quality-of-life improvements over a year.
How similar studies have gone: Small pilot studies, including the investigators' own 34-participant pilot, reported improvements in pain and anxiety but showed partial loss of benefit over months, and larger randomized trials of prolonged dog-assisted protocols remain limited.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age 18 years or older * Confirmed diagnosis of fibromyalgia * Being followed at ULS Alto Ave by the Multidisciplinary Pain Unit, Internal Medicine (Auto immune diseases), Physical and Rehabilitation Medicine or Neurology * Ability to read and write Portuguese and to understand the study procedures * Willingness and ability to participate voluntarily in the 10 session program and all scheduled assessments (T1-T4) * Provision of written informed consent Exclusion Criteria: * Allergy to dogs or marked fear of dogs * History of aggression towards animals * History of oncological disease * Concomitant systemic or rheumatologic disease that may confound pain and functional assessment * Decompensated psychiatric disorder or severe cognitive impairment that may compromise comprehension of the protocol or adherence to the intervention * Refusal to participate or withdrawal of consent at any point
Where it's running
-
Unidade Local de Saúde (ULS) Alto Ave
Guimarães, Portugal Recruiting
Study contacts
- Principal investigator: Filipa Martins-Alves, Psychiatric Hospital Assistant — Psychiatry Department, Unidade Local de Saúde (ULS) Alto Ave
- Study coordinator: Armando Almeida, Associate Professor
- Email: aalmeida@med.uminho.pt
- Phone: +351 936615717
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Whole-body Cryotherapy for Fatigue in ME/CFS, Fibromyalgia, Long COVID
This study tests whether brief, repeated exposure to extreme cold can help reduce fatigue and related symptoms in adults with ME/CFS, fibromyalgia, or Long COVID compared to healthy controls.
-
Noninvasive brain stimulation to see if it lowers pain in fibromyalgia
This study tests whether daily noninvasive brain stimulation can reduce pain and improve quality of life for people with fibromyalgia, using two brain targets and a crossover design.
-
Home-based high-dose tDCS for fibromyalgia: predicting response and comparing brain targets
This study tests whether a high-dose home-based tDCS treatment is at least as good as the conventional home-based tDCS for people with fibromyalgia, and whether it could be better, while also checking if baseline EEG can predict who responds.
-
Dietary strategies to help fibromyalgia in overweight or obese women
This trial tests whether a very low-calorie ketogenic diet, a Mediterranean diet, or a Mediterranean diet with a probiotic can reduce fibromyalgia symptoms in overweight or obese women.
-
Isokinetic microdose exercise for women with fibromyalgia
This 8-week program will test whether low-dose isokinetic exercise helps women with fibromyalgia reduce pain, improve strength, and enhance quality of life.
-
Does hardaliye help fibromyalgia when added to a personalized diet?
This study tests whether a traditional grape-based drink called hardaliye, used with a personalized diet, can improve symptoms and inflammation in adult women with fibromyalgia.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.